Final Procedures for Considering Requests Under the Commercial Availability Provision of the Dominican Republic-Central America-United States Free Trade Agreement, 13256-13264 [E7-5102]
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information under the provisions of the
Paperwork Reduction Act (44 U.S.C.
Chapter 35).
Agency: United States Patent and
Trademark Office (USPTO).
Title: Electronic Response to Office
Action and Preliminary Amendment
Forms.
Form Number(s): PTO Forms 1930,
1957, 1966.
Agency Approval Number: 0651–
0050.
Type of Request: Revision of a
currently approved collection.
Burden: 25,653 hours annually.
Number of Respondents: 150,900
responses per year.
Avg. Hours per Response: The time
needed to respond to the request for
reconsideration form is estimated to be
10 minutes (0.17 hours). This includes
time to gather the necessary
information, create the documents, and
submit the completed request.
Needs and Uses: This collection is
being submitted as a proposed addition
in support of a notice of proposed
rulemaking, ‘‘Changes in the
Requirements for Filing Requests for
Reconsideration of Final Office Action
in Trademark Cases’’ (RIN 0651–AC05).
The USPTO proposes to amend 37 CFR
2.64 to require a request for
reconsideration of an examining
attorney’s final refusal or requirement to
be filed through the Trademark
Electronic Application System (TEAS)
within three months of the mailing date
of the final action.
This rulemaking would add an
additional requirement to this
collection, a Request for
Reconsideration after Final Action
(Form 1930). The amendment to 37 CFR
2.64 would streamline and promote
efficiency in the process once a final
action has issued in an application for
Trademark registration. By setting a
three-month period in which to file a
request for reconsideration of the final
action, and by requiring that the request
be filed through TEAS, the proposed
amendment would facilitate the likely
disposition of an applicant’s request for
reconsideration prior to the six-month
deadline for filing an appeal to the
Trademark Trial and Appeal Board
(TTAB) or petition to the Director on the
same final action. This practice may
eliminate the need for some appeals or
petitions, and reduces the need for
remands and transfers of applications
on appeal.
The proposed earlier deadline and
mandatory TEAS filing facilitate the
likely disposition of the request for
reconsideration prior to the deadline to
petition or appeal. A grant of
reconsideration within this timeframe
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will obviate the need for an applicant to
file an appeal or petition, thus also
saving the applicant the filing fee for an
appeal or petition. A denial of
reconsideration within this timeframe
will obviate the need for a case on
appeal to be remanded and transferred
between the TTAB and the examining
attorney. Under either scenario, the
timeframe in the proposed rule
promotes more efficient and prompt
handling of the case, and achieves
benefits both for the applicant and the
USPTO.
Affected Public: Individuals or
households; business or other for-profit;
not-for-profit institutions.
Frequency: On occasion.
Respondent’s Obligation: Required to
obtain or retain benefits.
OMB Desk Officer: David Rostker,
(202) 395–3897.
Copies of the above information
collection proposal can be obtained by
any of the following methods:
• E-mail: Susan.Fawcett@uspto.gov.
Include ‘‘0651–0050 copy request’’ in
the subject line of the message.
• Fax: 571–273–0112, marked to the
attention of Susan Brown.
• Mail: Susan K. Brown, Records
Officer, Office of the Chief Information
Officer, Architecture, Engineering and
Technical Services, Data Architecture
and Services Division, U.S. Patent and
Trademark Office, P.O. Box 1450,
Alexandria, VA 22313–1450.
Written comments and
recommendations for the proposed
information collection should be sent on
or before April 20, 2007 to David
Rostker, OMB Desk Officer, Room
10202, New Executive Office Building,
Washington, DC 20503.
Dated: March 15, 2007.
Susan K. Brown,
Records Officer, USPTO, Office of the Chief
Information Officer, Architecture,
Engineering and Technical Services, Data
Architecture and Services Division.
[FR Doc. E7–5137 Filed 3–20–07; 8:45 am]
BILLING CODE 3510–16–P
COMMITTEE FOR THE
IMPLEMENTATION OF TEXTILE
AGREEMENTS
Final Procedures for Considering
Requests Under the Commercial
Availability Provision of the Dominican
Republic-Central America-United
States Free Trade Agreement
March 15, 2007.
Committee for the
Implementation of Textile Agreements
(CITA).
AGENCY:
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Summary and response to
comments concerning the CAFTA-DR
commercial availability interim
procedures; notice of final procedures.
ACTION:
SUMMARY: This notice summarizes the
comments received concerning the
Interim Procedures and provides
responses to those comments. See
Interim Procedures for Considering
Requests Under the Commercial
Availability Provision to the Dominican
Republic-Central America-United
States Free Trade Agreement, 71 FR
9315 (February 23, 2006).
EFFECTIVE DATE: The date of entry into
force of the Dominican-Central AmericaUnited States Free Trade Agreement.
FOR FURTHER INFORMATION CONTACT:
Richard Stetson, Office of Textiles and
Apparel, U.S. Department of Commerce,
(202) 482-3400.
SUPPLEMENTARY INFORMATION:
Authority: Section 203(o)(4) of the
Dominican Republic-Central America-United
States Free Trade Agreement Implementation
Act (‘‘CAFTA-DR’’); the Statement of
Administrative Action (‘‘SAA’’),
accompanying the CAFTA-DR, at 16-20.
Comments and Responses Concerning
the Interim Procedures
On February 21, 2006, the Committee
for the Implementation of Textile
Agreements (‘‘CITA’’) issued a Federal
Register notice advising interested
parties of Interim Procedures that CITA
would follow in implementing certain
provisions of the Dominican RepublicCentral America-United States Free
Trade Agreement Implementation Act
(‘‘CAFTA-DR Implementation Act’’),
namely the procedures for modification
of the list of fabrics, yarns or fibers not
available in commercial quantities in a
timely manner in the countries that are
Parties to the CAFTA-DR Agreement
(‘‘CAFTA-DR’’ or ‘‘Agreement’’), as set
out in Annex 3.25 of the CAFTA-DR.
CITA has reviewed and considered all
submitted comments, and below is a
summary of and response to those
comments.
Standards For Submissions: One
commentator noted that the interim
procedures did not provide a factual
standard for determining the
substitutability of other products for the
product subject to the commercial
availability request. See, e.g., sections
4(b)(4) and 6(b)(2)(iv) of the Interim
Procedures. CITA has not adopted this
suggestion. A wide range of products
may be the subject of a commercial
availability request. As each commercial
availability request is evaluated on the
basis of the facts contained therein, it
would be impracticable to set forth a
uniform standard for substitutability;
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rather, CITA will examine each request
and any subsequent responses on a caseby-case basis.
The same commentator suggested that
an offer made in response to a request
must contain an explicit commitment by
the potential CAFTA-DR supplier to
immediately deliver the product in
question or one determined to be
substitutable. CITA has not adopted this
suggestion. Section 203(o)(4)(C) of the
CAFTA-DR Implementation Act sets
forth the standard that the subject
product be delivered ‘‘in a timely
manner.’’ What is ‘‘timely’’ in any given
situation can only be determined on a
case-by-case basis.
One commentator asked that CITA
clarify that in addition to accepting
responses that object to a request, CITA
will also accept submissions in support
of a request. Section 203(o)(4)(C)(iii)(II)
of the CAFTA-DR Implementation Act
provides for a determination as to
whether any ‘‘interested entity has
objected to the request.’’ Section 6 of the
Interim Procedures required that an
objection to the request contain an offer
to supply, and that both offers to supply
and rebuttal submissions provide
information to substantiate the claims
contained in the respective submissions.
This requirement is maintained in
section 6 of the Final Procedures. Thus,
CITA will not consider submissions in
support of a request in making
commercial availability determinations.
Removal From Annex 3.25 List: One
commentator noted that the procedures
should contain an explicit statement
that all products already approved
under Trade Preference Programs
(Caribbean Basin Trade partnership Act
(‘‘CBTPA’’), African Growth and
Opportunity Act (‘‘AGOA’’), and the
Andean Trade Promotion and Drug
Eradication Act (‘‘ATPDEA’’) and added
to the list in Annex 3.25 of CAFTA-DR
cannot be removed from Annex 3.25. A
different commentator asked that CITA
confirm that products added to the list
in Annex 3.25 since the date that the
CAFTA-DR was signed cannot be
removed from that list. Article 3.25.5(a)
of the CAFTA-DR and section
203(o)(4)(E)(I) of the CAFTA-DR
Implementation Act provide that
fabrics, yarns, or fibers added to the list
in Annex 3.25 since the date the
CAFTA-DR was signed are subject to
removal. Section 9 of Final Procedures
accurately reflects these statutory
requirements.
Public Notice: One commentator
asserted that the procedures’ reliance on
Internet notification and electronic mail
(‘‘email’’) correspondence will result in
delays or failures to distribute the
information fully, especially for small
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companies relying on outside
consultants. Moreover, the commentator
stated that forbearing the use of a
Federal Register notification results in
greater risk for parties to be uninformed
of developments in these proceedings.
Another commentator alleges that as
these procedures are a federal
administrative process, publication in
the Federal Register is required so that
all parties may be assured of
notification. Given the abbreviated
timeline for these proceedings, Internet
and email communications provide
more timely notification than
publication in the Federal Register and
allow all parties equal opportunity for
notification. This is particularly relevant
for parties outside of the United States.
Further, given the abbreviated timeline
for such proceedings, Internet and email
communications provide interested
entities with more time to allocate to
reviewing information and providing
submissions than Federal Register
publication would allow. Moreover,
although a notice published in the
Federal Register does constitute ‘‘public
notice,’’ it is not the only means by
which to notify the public. CITA has
widely publicized that any interested
party may receive its email notifications
and that all public documents will be
posted on its website. This system
provides broad access and accessibility
to interested parties inside and outside
of the United States.
Another commentator noted that
CITA’s requirement to submit hard
copies of submissions via express
courier is too inflexible, and requests
that CITA accept hand-delivered
submissions accompanied by an
appropriate receipt that allows
confirmation of delivery. CITA has not
adopted this suggestion. In light of the
abbreviated timeline for such
proceedings, delivery by express courier
permits tracking of submissions and
avoids the possibility of documents
being lost or misplaced.
One commentator asked that CITA
accept submissions of electronic
information in PDF format. CITA has
adopted this suggestion and clarified
this point in the Final Procedures.
Other commentators asked that CITA
advise interested parties of all
deadlines, extensions, availability of
samples for public inspection, and the
posting of responses on the website in
its email notifications. Additional
commentators requested that the
procedures clarify that information on
determinations, including ‘‘Deemed
Approvals’’ and removal of restrictions
will be provided through email
notifications, website postings, and
publication in the Federal Register.
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CITA has adopted this suggestion and
clarified these points in its Final
Procedures.
Contents of Requests and Responses:
A commentator suggested that requests
should include ‘‘offers to buy,’’ as
responses are required to contain ‘‘offers
to supply,’’ to prevent speculative and
spurious requests by potential buyers.
CITA has not adopted this suggestion.
CITA has no authority to obligate or
compel requesters to purchase products,
and therefore, cannot require requesters
to include an ‘‘offer to buy.’’ However,
should a subject or substitutable
product be available from a CAFTA-DR
supplier, articles containing such
products from third-country sources
would not qualify for preferential trade
benefits.
Another commentator suggested that
denials, approvals in restricted
quantities, or removals contain contact
information of the potential CAFTA-DR
supplier(s) of the subject product(s).
This information would already be
contained in any response with an offer
to supply or rebuttal submission.
Moreover, as this information is posted
on the Internet, there is no need to
duplicate such information in CITA’s
determination notice.
The same commentators suggested
that responses with an offer to supply
should contain a sample of the
petitioned or allegedly substitutable
product. CITA is not adopting this
suggestion. CITA notes that given the
abbreviated timeline to conduct these
proceedings and depending on the
nature of the requested product, it may
not be possible for an interested entity
to provide a sample in all situations.
Samples may be submitted with
requests or offers to supply, but this is
not required. CITA notes that in the
event that the 14-day extension is
invoked, interested entities are provided
with additional time to provide a
sample product to substantiate their
claims should they choose to do so.
A commentator asked that CITA allow
discretion regarding treatment of
business confidential information in
special circumstances, such as when a
potential supplier wants to keep its
name confidential for fear of retaliation.
CITA has not adopted this suggestion. In
order to conduct this procedure in an
open and fair manner, CITA finds it is
necessary for all participants to know:
(1) the names of potential suppliers that
have been contacted by petitioners, and
(2) those interested entities who object
to the request. However, specific
proprietary information may be treated
as business confidential information.
See section 3 of the Final Procedures.
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Restricted Quantities: One
commentator was strongly opposed to
an automatic review of restricted
quantities in a CITA determination,
alleging that such reviews would
burden parties and CITA with
unnecessary processes. Moreover, this
commentator claims that the automatic
review is not required by the legislation.
Section 203(o)(4)(C)(vi) of the CAFTADR Implementation Act provides that
the restriction may be eliminated not
later than six months after the product
is added to the list in Annex 3.25 of the
Agreement in a restricted quantity.
Therefore, CITA may review current
circumstances to determine whether
eliminating the restricted quantity is
warranted. This section of the Final
Procedures has been revised to provide
clarity. See section 8(c)(3) of the Final
Procedures.
One commentator asked that CITA
specify how it will determine a given
quantity in determinations that involve
restricted quantities. In the course of the
proceeding, based on the information
submitted , CITA will specify an
amount that can be provided by the
CAFTA-DR supplier(s). CITA will
provide additional explanation in a
Frequently Asked Questions (‘‘FAQ’’)
document that will be made available
on its website.
Another commentator requests that in
section 8(c)(2) of the Interim
Procedures, regarding approvals in
unrestricted quantities, the language be
modified to read, ‘‘... if CITA determines
that no CAFTA-DR supplier(s) or
manufacturer(s) could fulfill any
amount of the request.’’ CITA has
determined to remove this sentence all
together, as it is redundant to the
previous sentence.
The same commentator asked that
CITA consider eliminating a quantity
restriction only upon receipt of a
request from an interested entity. CITA
has not adopted this suggestion. Section
203(o)(4)(C)(vi) of the CAFTA-DR
Implementation Act does not require
that a request be submitted to CITA, but
only that CITA may remove the
restriction within six months after the
product is added to the Annex 3.25 list
in a restricted quantity.
A commentator asked that CITA
clarify that approvals in restricted
quantities take effect 30 days after the
official receipt of the request. CITA is
required to make a determination,
whether a denial, approval in an
unrestricted quantity, or an approval in
a restricted quantity, within the 30 U.S.
business-day deadline, with the caveat
that CITA may extend the deadline for
an additional 14 U.S. business days
should additional information be
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required. See Section 8(c) of the Interim
and Final Procedures.
Another commentator asked that
CITA specify that the effective date of
the elimination of a restriction will be
six months after the date of publication
of the notice. CITA has not adopted this
suggestion. CITA notes that section
203(o)(4)(C)(vi) of the CAFTA-DR
Implementation Act does not specify the
effective date for removal of the
restricted quantity should CITA make
such a determination. CITA would
publish in the Federal Register any
modification to products on the Annex
3.25 list, such as removal of a
restriction, which in effect adds a
product to the Annex 3.25 list in an
unrestricted quantity. CITA notes that
section 203(o)(4)(C)(v) of the CAFTA-DR
Implementation Act specifies that the
effective date for adding products to the
Annex 3.25 list in an unrestricted or
restricted quantity is the date of
publication in the Federal Register.
A commentator asked that CITA
clarify that a review to determine
whether to remove restricted quantities
can take place later than six months
after adding the product in a restricted
quantity to the Annex 3.25 list. CITA
has not adopted this suggestion. The
procedure in section 8(c)(3)(ii) of the
Final Procedures implements Section
203(o)(4)(C)(vi) of the CAFTA-DR
Implementation Act which provides
only for a review not later than six
months after the product is added to the
Annex 3.25 list in a restricted quantity.
Changed Circumstances: Several
commentators requested that CITA
clarify a discrepancy in the timeframes
provided for reconsideration of
determinations in sections 8(c)(6) and
9(a) of the interim procedures. Another
commenter requested that CITA strike
section 8(c)(6).
In section 8(c)(6) of the Interim
Procedures, CITA proposed to allow for
proceedings based upon changed
circumstances. Several commentators
expressed that CITA does not possess
statutory authority to conduct changed
circumstances proceedings. The Final
Procedures clarify when it is
appropriate for the agency to conduct a
proceeding based upon changed
circumstances. It is CITA’s intention at
this time to exercise its inherent
authority to reconsider, and/or
subsequently amend, commercial
availability determinations that may
have been procured by, e.g., error, fraud,
or similar faults. See, e.g., Elkem
Metals, et al. v. United States, 26 C.I.T.
234, 239, 193 F. Supp. 2d 1314, 131920 (2002) (‘‘It is indeed the general rule
that administrative agencies in
general...have the inherent authority to
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institute reconsideration proceedings so
as to ‘vindicate the integrity of the
administrative process.’’’); Belville Min.
Co. v. U.S., 999 F.2d 989, 997 (6th Cir.
1993) (‘‘Even where there is no express
reconsideration authority for an
agency...the general rule is that an
agency has inherent authority to
reconsider its decision, provided that
reconsideration occurs within a
reasonable time after the first
decision.’’)(citations and internal
quotations omitted)); Bookman v.
United States, 197 Ct. Cl. 108, 453 F.2d
1263, 1265 (1972) (explaining the
general rule that ‘‘every tribunal,
judicial or administrative, has some
power to correct its own errors or
otherwise modify its judgment, decree,
or order’’ and that ‘‘[courts] will sustain
the reconsidered decision of an agency,
as long as the administrative action is
conducted within a short and
reasonable time’’) (citations and internal
quotations omitted)); Gilmore Steel
Corp. v. U.S., 7 C.I.T. 219, 223, 585 F.
Supp. 670, 674 (1984) (holding that the
International Trade Administration had
the authority to correct a manifest error
that ‘‘taints the proceeding’’); Gun
South, Inc. v. Brady, 877 F.2d 858, 862
(11th Cir. 1989) (concluding that the
Bureau of Alcohol, Tobacco, and
Firearms ‘‘must necessarily retain the
power to correct the erroneous approval
of firearms import applications’’ despite
the absence of express statutory
authority).
Therefore, the proposed changed
circumstances provision was not based
on statutory changes made by the
CAFTA-DR Implementation Act, but
rather relied on the longstanding
inherent authority that CITA has always
possessed. See cases cited supra.
Further, neither the CAFTA-DR
Implementation Act nor case precedent
prohibits the proposed proceeding. In
the interest of fairness and transparency,
however, it seems appropriate to clarify
the agency’s inherent authority to
address such faults in the conduct of the
proceeding. In the Final Procedures,
CITA has deleted section 8(c)(6) and
provided a clarification in the
‘‘Background’’ section.
Deadlines: Several commentators
noted that the deadlines set forth by the
procedures do not allow for extensions
for responses with offers to supply or
rebuttal comments. The procedures do
allow for CITA to extend the time limit
for responses with offers to supply and
rebuttal comments. However, even if an
extension is provided, CITA is required
to meet the statutory deadline for
making a determination. See sections 6
and 7of the Final Procedures; see also,
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e.g., section 203(o)(4)(C)(iv) of the
CAFTA-DR Implementation Act.
Another commentator suggested that
CITA begin the timeline for the
proceeding from the date of publication
of the commercial availability request
rather than the date of its official receipt
by CITA, which would allow for two
additional days for submitting responses
with offers to supply. CITA has not
adopted this suggestion, as CITA needs
sufficient time to review the
completeness of commercial availability
requests before notifying interested
parties that a commercial availability
request has been submitted and
accepted. At the same time, the statute
requires that the determination be made
within a certain time period from the
date of submission. Therefore, in order
for CITA to make a commercial
availability determination within the
statutorily prescribed deadlines, CITA
needs the two days in question to
review the completeness of the
commercial availability request before
notifying interested parties that a
request has been submitted and
accepted. See section 203(o)(4)(C)(iv) of
the CAFTA-DR Implementation Act.
Another commentator suggested that
when CITA seeks to meet with
interested entities during an extended
review period, the meeting should
include all sides of the issue and be
open to the public. Should CITA
convene a meeting between the
requester and interested entities
providing offers to supply, such
meetings will be public and conducted
in an open manner.
A commentator explained that the
procedures should state that CITA may
determine to extend the 30-day deadline
for an additional 14 days to obtain
additional information. Section 8 of the
Final Procedures explains that CITA is
permitted to extend the 30 U.S.
business-day deadline for an additional
14 U.S. business days. This same
section of the procedures clearly
explains the purpose of the 14 U.S.
business day extension. See also section
203(o)(4)(c)(iv) of the CAFTA-DR
Implementation Act.
Another commentator asked that
CITA add in section 8(c)(3)(i) of the
Interim Procedures the phrase, ‘‘or not
more than 44 U.S. business days where
extension is provided...’’ CITA has
adopted this suggestion in its Final
Procedures.
A commentator requested that CITA
clarify that if CITA provides an
extension for submitting responses with
offers to supply, CITA’s determinations
will still meet the statutory deadline.
CITA has adopted this suggestion in its
Final Procedures.
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One commentator asked that CITA
acknowledge that in ‘‘emergency
circumstances’’ CITA could make a
decision prior to its 30 U.S. businessday deadline. CITA has not adopted this
suggestion. CITA is required to make a
determination ‘‘within’’ 30 U.S.
business days of receipt of a commercial
availability request, unless an extension
is provided. See section 203(o)(4)(C)(iv)
of the CAFTA-DR Implementation Act.
Moreover, each proceeding must allow
all interested entities sufficient time to
respond with offers to supply and
provide rebuttal comments in the course
of the proceeding.
Deemed Approval: One commentator
objected to the provision regarding
‘‘Deemed Approval,’’ noting that such
requirements set a negative precedent
for future procedures. CITA has not
adopted this suggestion. Section
203(o)(4)(D) of the CAFTA-DR
Implementation Act provides expressly
for the ‘‘Deemed Approval’’ procedure.
Another commentator asked that the
‘‘Deemed Approval’’ provision apply to
all determinations in these proceedings,
not only to commercial availability
requests to add a given product to
Annex 3.25. Section 203(o)(4)(D) of the
CAFTA-DR Implementation Act
provides that the ‘‘Deemed Approval’’
process only applies to commercial
availability requests and not to requests
to remove or restrict.
Interested Entities: One commentator
claimed that CITA inadvertently limited
participation in commercial availability
proceedings by using the term
‘‘interested entities’’ to identify who
may request to be included on the email
notification list. The Final Procedures
clarify that any interested party can be
included on the mass email notification
list.
Another commentator asked that
CITA clarify that trade associations are
an ‘‘interested entity.’’ CITA has not
adopted this suggestion. The term
‘‘interested entity’’ is defined in section
203(o)(4)(B)(i) of the CAFTA-DR
Implementation Act, and this definition
does not include trade associations.
However, trade associations can
participate in the process as an
interested party.
A commentator noted that the
language of the procedures differs from
the Agreement and the CAFTA-DR
Implementation Act, using the standard
for determining whether to add a
product to the Annex 3.25 list as ‘‘are
not available’’ instead of ‘‘are available’’
in the CAFTA-DR countries. The
language of the procedures is consistent
with both the Agreement and the
CAFTA-DR Implementation Act.
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One commentator asked that CITA
clarify that non-essential character
components are eligible for
determinations. The CAFTA-DR
Implementation Act provides for
determinations whether ‘‘fabrics, yarns,
or fibers’’ are to be added to the list in
Annex 3.25 of the Agreement. See
section 203(o)(4)(A). Further, Section
Notes 2, 3, and 4 to Section XI of Annex
4.1 of the Agreement provides for how
the list of fabrics, yarns, and fibers in
Annex 3.25 is taken into account in
applying the Agreement’s rules of
origin. Nothing in the commercial
availability process alters the rules of
origin contained in the Agreement.
Several commentators asked that
CITA elaborate on several of the
provisions included in the procedures,
including ‘‘Deemed Approval,’’
approvals with restricted quantities, the
contents of commercial availability
requests, responses with offers to
supply, and rebuttal comments. CITA
has adopted this suggestion and will
provide further explanations in a FAQ
document to be made available on its
website.
Another commentator asked that
CITA review its procedures after one
year to determine if any modifications
are necessary. The Final Procedures
provide that the procedures may be
modified at any time to address
concerns that may arise. CITA notes that
these are administrative procedures
rather than regulations, and can be
modified as needed.
Final Procedures
This notice also sets forth the final
procedures the Committee for the
Implementation of Textile Agreements
(‘‘CITA’’) will follow in implementing
certain provisions of the Dominican
Republic-Central America-United States
Free Trade Agreement Implementation
Act (‘‘CAFTA-DR Implementation Act’’).
Section 203(o)(4) of the CAFTA-DR
Implementation Act establishes
procedures for the President to modify
the list of fabrics, yarns, or fibers not
available in commercial quantities in a
timely manner in the countries that are
Parties to the CAFTA-DR, as set out in
Annex 3.25 of the Agreement. The
President has delegated to CITA the
authority to determine whether a fabric,
yarn, or fiber is not available in
commercial quantities in a timely
manner in CAFTA-DR countries and has
directed CITA to establish procedures
that govern the submission of a request
and provide the opportunity for
interested entities to submit comments
and supporting evidence in any such
determination pursuant to the CAFTADR Implementation Act. This notice
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hereby gives notice to interested parties
of the procedures CITA will follow in
considering such requests.
Background:
The CAFTA-DR provides a list in
Annex 3.25 of the Agreement for fabrics,
yarns, and fibers that the Parties to the
Agreement have determined are not
available in commercial quantities in a
timely manner from suppliers in the
United States or other CAFTA-DR
countries. A textile and apparel good
containing fabrics, yarns, or fibers that
is included in Annex 3.25 of the
Agreement may be treated as if it is an
originating good for purposes of the
specific rules of origin in Annex 4.1 of
the Agreement, regardless of the actual
origin of those inputs, provided that all
other fabrics, yarns, or fibers of the
component that determines the
classification of the good meet the
specific rules of origin in Annex 4.1 of
the Agreement. The CAFTA-DR
Implementation Act provides that the
President will establish procedures
governing the submission of requests
and may determine whether additional
fabrics, yarns, or fibers are not available
in commercial quantities in a timely
manner in the United States or the other
CAFTA-DR countries. In addition, the
CAFTA-DR Implementation Act
establishes that the President may
remove a fabric, yarn, or fiber from the
list, if it has been added to the list in
an unrestricted quantity pursuant to
section 203(o), if he determines that the
fabric, yarn, or fiber has become
available in commercial quantities in a
timely manner.
The SAA provides that the President
will delegate to CITA his authority
under section 203(o)(4) of the
Agreement (‘‘Commercial Availability
Provision’’), to establish procedures for
modifying the list of fabrics, yarns, or
fibers not available in commercial
quantities in a timely manner for
Agreement countries, as set out in
Annex 3.25 of the Agreement.
These procedures are not subject to
the requirement to provide prior notice
and opportunity for public comment,
pursuant to 5 U.S.C. 553(b)(A)
(Administrative Procedures Act). These
procedures may be modified in the
future to address concerns that may
arise as CITA gains experience in
implementing them. CITA possesses
inherent authority to reconsider, and/or
subsequently amend, commercial
availability determinations that may
have been procured by error, fraud, or
similar faults. Should CITA undertake
to review a determination under such
circumstances, CITA will provide notice
to the public, through the email and
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website notification processes described
in the Final Procedures, and provide
opportunity for interested entities to
submit comments and information for
CITA’s consideration.
Procedures for Considering Requests
1. Introduction
The intent of the CAFTA-DR
Commercial Availability Procedures is
to foster the use of U.S. and CAFTA-DR
products by implementing procedures
that allow products to be placed on or
removed from a product list, on a timely
basis, and in a manner that is consistent
with normal business practice. To this
end, these procedures are intended to
facilitate the transmission, on a timely
basis, of order requests and offers to
supply such requests; have the market
indicate the availability of the supply of
products that are the subject of requests;
make available promptly, to interested
entities and parties, information
regarding the requests for products and
offers to supply received; ensure wide
participation by interested entities and
parties; provide careful scrutiny of
information provided to substantiate
order requests and response to supply
offers; and provide timely public
dissemination of information used by
CITA in making commercial availability
determinations.
2. Definitions
(a) Commercial Availability Request. A
‘‘Commercial Availability Request’’ is a
submission from an interested entity
requesting that CITA place a good on
the list in Annex 3.25 because that fiber,
yarn, or fabric is not available in
commercial quantities in a timely
manner from a supplier in the CAFTADR countries.
(b) Interested Entity. An ‘‘interested
entity’’ means a government that is a
Party to the Agreement, other than the
United States; a potential or actual
purchaser of a textile or apparel good;
or a potential or actual supplier of a
textile or apparel good. CITA recognizes
that a legal or other representative may
act on behalf of an ‘interested entity.’
See section 203(o)(4)(B)(i) of the
CAFTA-DR Implementation Act.
(c) Interested Party. An ‘‘interested
party’’ means any interested person that
requests to be included on the email
notification list for Commercial
Availability proceedings. Any interested
person may become an interested party
by contacting CITA. See Office of
Textile and Apparel, U.S. Department of
Commerce, website for details at https://
web.ita.doc.gov/tacgi/CABroadcast.nsf/
Document?Openform or send an email
to OTEXACAFTA@ita.doc.gov.
(d) Official Receipt. The ‘‘official
receipt’’ is CITA’s email confirmation
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that it has received both the email
version and the original submission
signed by the interested entity delivered
via express courier.
(e) Request. A ‘‘request’’ refers to the
Commercial Availability Request.
(f) Request to Remove or Restrict. A
‘‘request to remove or restrict’’ is a
submission from an interested entity,
made no sooner than six months after a
product has been added to the Annex
3.25 list in an unrestricted quantity
pursuant to Section 203(o) of the
CAFTA-DR Implementation Act,
requesting that CITA either remove a
product or that a quantity restriction be
introduced.
(g) Requestor. The ‘‘requestor’’ refers to
the interested entity that files a request,
either a Commercial Availability
Request or a Request to Remove or
Restrict, under the CAFTA-DR
Commercial Availability provision, for
CITA’s consideration.
(h) CAFTA-DR Supplier. A ‘‘CAFTA-DR
supplier’’ is a potential or actual
supplier of a textile or apparel good in
the territory of any Party.
(i) Response with an Offer. A ‘‘response
with an offer’’ is a submission from an
interested entity to CITA providing its
objection to the request or asserting its
ability to supply the subject product by
providing an offer to supply the subject
product described in the request.
(j) Rebuttal Comment. A ‘‘rebuttal
comment’’ is a submission from an
interested entity providing information
in response to evidence or arguments
raised in a response with an offer
submission. Rebuttal comments must be
limited to evidence and arguments
provided in a response with an offer
submission.
(k) Fiber, Yarn, or Fabric. The term
‘‘fiber, yarn, or fabric’’ means a single
product or a range of products, which
meet the same specifications provided
in a submission, and which may be only
part of a Harmonized Tariff Schedule of
the United States (‘‘HTSUS’’) provision.
(l) U.S. Business Day. A ‘‘U.S. businessday’’ is any calendar day other than a
Saturday, Sunday, or a legal holiday.
See section 203(o)(4)(B)(i) of the
CAFTA-DR Implementation Act.
3. Submissions for Participation the
CAFTA-DR Commercial Availability
Proceeding.
(a) Filing a Submission.All submissions
for a CAFTA-DR Commercial
Availability proceeding (e.g.,
Commercial Availability Request,
Response with an Offer, Rebuttal
Comments, and Request to Remove or
Restrict) must be in English. If any
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attachments are in a language other than
English, then a translation must be
provided. Each submission must be
submitted to the U.S. Department of
Commerce’s Office of Textiles and
Apparel (‘‘OTEXA’’) in two forms,
electronic mail and original signed
submission.
(1) An electronic mail (‘‘email’’) version
of the submission must be either in
PDF, Word, or Word-Perfect format
and must contain an adequate
public summary of any business
confidential information and the
due diligence certification, sent to
OTEXAlCAFTA@ita.doc.gov. The
‘‘email’’ version of the submission
will be posted for public review on
OTEXA’s CAFTA-DR Commercial
Availability website at
http:otexa.ita.doc.gov. No business
proprietary information should be
submitted in the ‘‘email’’ version of
any document.
(2) The original signed submission must
be received via express courier to—
Chairman, Committee for the
Implementation of Textile
Agreements, Room H3100, U.S.
Department of Commerce, 14th and
Constitution Ave., N.W.,
Washington, DC 20230. Any
business confidential information
upon which an interested entity
wishes to rely must be included in
the original signed submission only.
Except for the inclusion of business
confidential information, the two
versions of a submission should be
identical.
(3) Brackets must be placed around all
business confidential information
contained in submissions.
Documents containing business
confidential information must have
a bolded heading stating
‘‘Confidential Version.’’
Attachments considered business
confidential information must have
a heading stating ‘‘Business
Confidential Information.’’
Documents, including those
submitted via ‘‘email,’’ provided for
public release, must have a bolded
heading stating ‘‘Public Version’’
and all the business confidential
information must be deleted and
substituted with asterisks.
(4) Generally, details, such as quantities
and lead times for providing the
subject product, can be treated as
business confidential information.
However, the names of suppliers
who were contacted, what was
asked generally about the capability
to manufacture the subject product,
and the responses thereto should be
included in public versions, which
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will be made available to the
public.
(b) Due Diligence Certification. An
interested entity must file a certification
of due diligence as described in
subsection (b)(1) with each submission,
both email and original signed versions,
containing factual information. If the
interested entity has legal counsel or
other representative, the legal counsel or
other representative must file a
certification of due diligence as
described in subsection (b)(2) with each
submission, both email and original
signed versions, containing factual
information. Accurate representations of
material facts submitted to CITA for the
CAFTA-DR Commercial Availability
proceeding are vital to the integrity of
this process and are necessary for
CITA’s effective administration of the
statutory scheme. Each submission
containing factual information for
CITA’s consideration must be
accompanied by the appropriate
certification regarding the accuracy of
the factual information. Any submission
that lacks the applicable certifications
will be considered an incomplete
submission that CITA will reject and
return to the submitter. CITA may verify
any factual information submitted by
interested entities in a CAFTA-DR
Commercial Availability proceeding.
(1) For the person responsible for
presentation of the factual
information: I, (name and title),
currently employed by (interested
entity), certify that (1) I have read
the attached submission, and (2) the
information contained in this
submission is, to the best of my
knowledge, complete and accurate.
(2) For the person’s legal counsel or
other representative:I, (name), of
(law or other firm), counsel or
representative to (interested entity),
certify that (1) I have read the
attached submission, and (2) based
on the information made available
to me by (person), I have no reason
to believe that this submission
contains any material
misrepresentation or omission of
fact.
(c) Official Receipt. A submission will
be considered officially submitted to
CITA only when both the email version
and the original signed submission have
been received by CITA. For request
submissions, CITA will confirm to the
requestor that both versions of the
request submission were received
through an email confirmation. CITA’s
email confirmation shall be considered
the ‘‘official receipt’’ of the request
submission, and also begins the
statutory 30 U.S. business-day process
for CITA consideration of requests.
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CITA will confirm official receipt of
response and rebuttal submissions by
posting the response or rebuttal on the
dedicated website at https://
web.ita.doc.gov/tacgi/
CaftaReqTrack.nsf.
4. Submitting a Request for
Consideration in a Commercial
Availability Proceeding.
(a) Commercial Availability Request. An
interested entity may submit a
Commercial Availability request to
CITA alleging that a fiber, yarn, or fabric
is not available in commercial quantities
in a timely manner from a producer in
the CAFTA-DR countries.
(b) Contents of a Commercial
Availability Request.
(1) Detailed Product Information. The
Commercial Availability request
must provide a detailed description
of the product subject to the
request, including, if applicable,
fiber content, construction, yarn
size, and finishing processes; and
the classification of the product
under the HTSUS. All
measurements in the entire
submission must be stated in metric
units, or if the English count system
is used in any part, then a
conversion to metric units must be
provided.
(2) Quantity. The Commercial
Availability request must provide
the specific quantity of the product
needed by the requestor, in
standard units of quantity for
production of the subject product in
the CAFTA-DR countries.
3) Due Diligence. The Commercial
Availability request must provide a
complete description of the due
diligence undertaken by the
requestor to determine the subject
product’s availability in the
CAFTA-DR countries. Due diligence
for the requestor means it has made
reasonable efforts to obtain the
subject product from CAFTA-DR
suppliers. The requestor must
provide the names and addresses of
suppliers contacted, who was
specifically contacted, the exact
request that was made, the dates of
those contacts, whether a sample of
the subject product was provided
for review, and the exact response
given for the supplier’s inability to
supply the subject product under
the same conditions as contained in
the Commercial Availability request
submitted to CITA, in addition to
any other information the requestor
believes is relevant. The requestor
must submit copies or notes of
relevant correspondence, both
inquiries and responses, with these
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suppliers. Relevant correspondence
includes notes of telephone
conversations. Specific details of
correspondence with suppliers,
such as quantities and lead times
for providing the subject product,
can be treated as business
confidential information. However,
the names of CAFTA-DR suppliers
who were contacted, what was
asked generally about the capability
to manufacture the subject product,
and the responses thereto should be
available for public review to
ensure proper public participation
in the process. ‘‘Lead times’’ refers
to supplying the subject product
within normal business time frames
for the subject product once an
order is received. Specific delivery
dates are not necessary. Required
delivery dates that fall within the
time needed to complete the
Commercial Availability
determination process are not
acceptable.
(4) Substitutable Products. The
Commercial Availability request
must provide information on
whether the requester believes that
other products supplied by the
CAFTA-DR supplier are not
substitutable in commercial
quantities in a timely manner for
the product(s) that is (are) the
subject of the request for purposes
of the intended use. Clearly
describe the unique characteristics
of the subject product that
distinguishes it from other similar
or potentially substitutable
products. Describe why such
characteristics are required for the
purposes of the end-use of the
product and cannot be substituted
by another product available from a
CAFTA-DR supplier.
(5) Additional Information. The
Commercial Availability request
may provide any additional
evidence or information believed to
be relevant for CITA to determine
whether a fiber, yarn, or fabric is
not available in commercial
quantities in a timely manner from
a producer in the CAFTA-DR
countries.
5. Consideration and Acceptance of a
Request.
In considering whether to accept a
request, CITA will consider and
determine whether it provides all the
required information specified in
sections 3 and 4 of these procedures.
CITA will determine whether to accept
the request for consideration and
investigation not later than two U.S.
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business days after the official receipt of
a request.
(a) Request Rejected. If CITA determines
that the request does not contain the
required information, the requestor will
be notified promptly by email that the
request has not been accepted and the
reasons for the rejection. A request may
be resubmitted with additional
information for the subject product and
CITA will reevaluate it as a new request.
(b) Request Accepted. If CITA
determines that the request contains the
required information, CITA will notify
interested parties by email that a request
has been accepted and filed and will
assign a File Number. CITA will post
the accepted request on its website for
public notice. The email notification
and the website posting will indicate
the calendar date deadlines for
submitting offers to supply and
submitting rebuttal responses.
6. Submitting a Response with an Offer
in a Commercial Availability
Proceeding.
Respondents must meet the
requirements outlined in 3 of these
procedures. General comments in
support of or opposition to a
commercial availability request do not
meet the requirements of a Response
with an Offer. A Due Diligence
Certification must accompany a
Response with an Offer.
(a) Response With an Offer Submission.
An interested entity may file a response
submission to a request CITA accepted
advising CITA of its objection to the
request and its ability to supply the
subject product by providing an offer to
supply the subject product as described
in the request. An interested entity will
have 10 U.S. business days after official
receipt of a request to respond to a
request. If good cause is shown, CITA
may extend this deadline, but CITA will
still meet the statutory deadline for
making a determination.
(b) Contents of a Response with an Offer.
(1) File Number. The Response with an
Offer needs to reference the CITA
File Number assigned to the
particular Commercial Availability
Request being addressed.
(2) Quantity. The Response with an
Offer must supply the quantity of
the requested subject product that
the CAFTA-DR supplier, is capable
of currently supplying, in standard
units of quantity. All measurements
must be in metric units. If the
English count system is used in any
part, then a conversion to metric
units must be provided.
(3) Production Capability. The Response
with an Offer must report the
quantity, in metric units, that the
CAFTA-DR supplier produced of
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the subject product, or a
substitutable product, in the
preceding 24-month period.
(i) For products that have experienced
cyclical demand or are not
currently produced, the CAFTA-DR
supplier should indicate the
quantity that has been supplied or
offered commercially in the past,
with an explanation of the reasons
it is not currently produced or
offered.
(ii) If the requestor has requested a
new style, weight, or other variation
that is new to the market or new to
the respondent, then the CAFTADR supplier(s) should provide
detailed information on its current
ability to make the subject product.
(iii) If the CAFTA-DR supplier(s) are
making a new product that has not
yet been offered to the market, but
could meet the requirements of the
subject product, then the CAFTADR supplier(s) need(s) to provide
detailed information regarding the
product and their ability to meet a
request.
(iv) Substitutable Products. The
Response with an Offer may
provide, if relevant, the basis for the
responder’s belief that other
products that are supplied by the
CAFTA-DR supplier in commercial
quantities in a timely manner are
substitutable for the product(s) that
are the subject of the request for
purposes of the intended use.
(4) Due Diligence. The Response with an
Offer must provide a complete
description of the due diligence
undertaken by the CAFTA-DR
supplier to substantiate the ability
to supply the subject product.
(i) In the case of new variations of a
product, the CAFTA-DR supplier
must substantiate the ability to
manufacture the subject product.
The CAFTA-DR supplier must
provide sufficient detail of the
manufacturing capabilities of the
facility that will supply the subject
product, in addition to any other
information the supplier believes is
relevant.
(ii) If some operations, such as
finishing, will be completed by
other entities, the name of the
facility and contact information
must be provided.
(5) Location of the CAFTA-DR supplier.
The Response with an Offer must
provide the name, address, phone
number, and email address of a
contact person at the facility
claimed to be able to supply the
subject product.
7. Submitting Rebuttal Comments.
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Rebuttal Comments must meet the
requirements outlined in 3 of these
procedures. General comments in
support of or opposition to a Request or
a Response with an Offer do not meet
the requirements of a Rebuttal
Comment. A Due Diligence Certification
must accompany a Rebuttal Comment.
(a) Rebuttal Comments. Any interested
entity may submit a Rebuttal Comment
to a Response with an Offer submission.
An interested entity must submit its
Rebuttal Comment not later than 4 U.S.
business-days after the deadline for
Response with an Offer submission. If
good cause is shown, CITA may extend
the time limit, but CITA will still meet
the statutory deadline for making a
determination.
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(b) Contents of a Rebuttal Comment. The
Rebuttal Comment may respond only to
evidence or arguments raised in the
Response with an Offer submission and
must identify the Response with an
Offer submission, evidence and/or
arguments to which it is responding.
The Rebuttal Comment needs to
reference the CITA File Number
assigned to the particular Commercial
Availability Request being addressed.
8. Determination Process.
(a) Not later than 30 U.S. business days
after official receipt of a request (or not
later than 44 U.S. business days where
an extension is provided), CITA will
notify interested entities by email and
interested parties and the public by a
posting on its website whether the
subject product is available in
commercial quantities in a timely
manner in the CAFTA-DR countries and
whether an interested entity has
objected to the request.
(b) CITA will notify the public of the
determination by publication in the
Federal Register when the
determination results in a change to the
Commercial Availability List in Annex
3.25 of the Agreement.
(c) Types of Determinations.
(1) Denial. A denial means that CITA
has determined that the subject
product is available in commercial
quantities in a timely manner in the
CAFTA-DR countries. If a request is
denied, notice of the denial will be
posted on the CAFTA-DR
Commercial Availability website at
https://web.ita.doc.gov/tacgi/
CABroadcast.nsf/
Document?Openform.
(2) Approval in Unrestricted Quantity.
An approval in unrestricted
quantities means that CITA has
determined that the subject product
is not available in commercial
quantities in a timely manner in the
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CAFTA-DR countries or that no
interested entity has objected to the
request.
(i) If a request is approved without
restriction, a notice will be
published in the U.S. Federal
Register not later than 30 U.S.
business days (or not more than 44
U.S. business days where an
extension is provided ) after the
official receipt of a request, adding
the subject product to the
Commercial Availability List in
Annex 3.25 of the Agreement.
(ii) The effective date of the
determination is the date of
publication of the notice in the U.S.
Federal Register.
(3) Approval in a Restricted Quantity.
(i) Approval in a Restricted Quantity.
An Approval in a Restricted
Quantity means that CITA has
determined to add the subject
product to the Commercial
Availability List in Annex 3.25 of
the Agreement with a specified
restricted quantity. CITA may
approve the request in a restricted
quantity if CITA determines that a
CAFTA-DR supplier(s) can partially
fulfill the request for the subject
product. The restricted quantity
specifies the amount of the subject
product that can be provided by a
CAFTA-DR supplier(s).
(A) If a request is approved in a
restricted quantity, a notice will be
published in the Federal Register
not later than 30 U.S. business days
(or not more the 44 U.S. business
days where an extension is
provided ) after official receipt of
the request, adding the subject
product to the Commercial
Availability List in Annex 3.25 of
the Agreement with a specified
restricted quantity. The restricted
quantity specifies the amount of the
subject product that can be
provided by a CAFTA-DR
supplier(s).
(B) The effective date of the
determination will be the date of
publication in the U.S. Federal
Register.
(ii) Elimination of a restricted
quantity. Not later than six months
after adding a product to the
Commercial Availability List in
Annex 3.25 of the Agreement in a
restricted quantity, CITA may
eliminate the restriction if it
determines that the subject product
is not available in commercial
quantities in a timely manner in the
CAFTA-DR countries.
(A) The determination that the subject
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13263
product is not available in
commercial quantities in a timely
manner will be based upon whether
the restricted quantity has been
provided by a CAFTA-DR
supplier(s). CITA will solicit
comments and information from the
CAFTA-DR supplier(s) and the
requester.
(B) If the CAFTA-DR supplier(s) are
still capable of providing the
restricted quantity, the restriction
will remain.
(C) If the CAFTA-DR supplier(s) are
unable to provide the restricted
quantity, CITA will eliminate the
restricted quantity. CITA will
publish a notice in the U.S. Federal
Register, and post on the website,
that the restricted quantity is
eliminated and the subject product
is added to the Commercial
Availability List in Annex 3.25 in
an unrestricted quantity. The
effective date of the determination
will be the date of publication in
the U.S. Federal Register.
(4) Insufficient Information to
Determine.CITA will extend its
time period for consideration of the
Commercial Availability Request by
an additional 14 U.S. business days
in the event that CITA determines,
not later than 30 U.S. business days
after official receipt of a
Commercial Availability Request,
that it has insufficient information
to make a determination regarding
the ability of a CAFTA-DR supplier
to supply the subject products of
the Commercial Availability
Request based on the submitted
information. CITA will normally
determine that it does not have
sufficient information to make a
determination on a Commercial
Availability Request when CITA
finds there is inconsistency in
material information contained in
the Commercial Availability
Request, one or more Offers to
Supply the subject product, and/or
the Rebuttal Comments. CITA will
notify interested parties via email
that it has extended the time period
for CITA’s consideration by 14 U.S.
business-days. CITA also will
announce the extension on the
website.
(i) Process during Extension Period.
During the extended time period,
CITA will request that interested
entities provide additional evidence
to substantiate the information
provided, and may initiate a
meeting with interested entities.
Should CITA elect to conduct a
meeting, it will comply with
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requirements to conduct
proceedings in an open manner.
Such evidence may include inter
alia product samples, lab tests,
detailed descriptions of product
facilities, and comparisons of
product performance in the
intended end-use of the subject
product. Any samples, if requested,
of fibers, yarns, or fabrics, that are
provided to CITA will be made
available for public inspection at
the Office of Textiles and Apparel,
Room 3110, U.S. Department of
Commerce, 14th St. and
Constitution Ave., N.W.,
Washington, DC 20230. All written
submissions must follow
instructions described in section 3
of these procedures. Samples
should be identified with a cover
sheet that describes the
specifications of the sample and be
identical to the specifications of the
request.
(ii) CITA also will consider evidence
in support of claims that CAFTADR supplier(s) can supply a
substantially similar product to that
specified in the request.
(iii) CITA will make a determination,
not later than 44 U.S. business days
after the official receipt of a
Commercial Availability Request
whether to Approve, Approve with
Restriction, or Deny the
Commercial Availability Request
and will follow the notification
process accordingly.
(5) Deemed Approval. In the event that
CITA does not make a
determination in response to a
Commercial Availability Request to
add a product to Annex 3.25 of the
Agreement within the statutory
deadlines provided, not later than
45 U.S. business-days after the
official receipt of the commercial
availability request or not later than
60 U.S. business-days after the
official receipt of the Commercial
Availability Request that was
determined to lack sufficient
information pursuant to subsection
(c)(4), the requested subject product
shall be added to the Commercial
Availability List in Annex 3.25 , in
an unrestricted quantity, in
accordance with the requirements
of section 203(o)(4)(D) of the
CAFTA-DR Implementation Act.
CITA will notify the public of the
Deemed Approval by publication in
the U.S. Federal Register and
posting on OTEXA’s website.
9. Six Month Procedures:
(a) Request to Remove or Restrict. No
earlier than six months after a product
has been added to the Commercial
VerDate Aug<31>2005
17:08 Mar 20, 2007
Jkt 211001
Availability List in Annex 3.25 in an
unrestricted quantity pursuant to
sections 203(o)(2) and (4) of the CAFTADR Implementation Act, an interested
entity may submit a request to CITA
requesting that a product be either
removed or that a quantity restriction be
introduced.
(b) Content of a Request to Remove or
Restrict. The Request to Remove or
Restrict must provide the substantive
information set forth in subsection 6(b)
(Contents of a Response with an Offer)
of these procedures.
(c) Procedures.
(1) In considering whether to accept a
Request to Remove or Restrict,
CITA will follow procedures set
forth in section 5 (Consideration
and Acceptance of a Request) of
these procedures.
(2) If CITA determines to accept the
Request to Remove or Restrict,
CITA and any responding interested
entity shall follow applicable
procedures and contents set forth in
subsections 6(a) (Response
Submission) and section 7
(Submitting Rebuttal Evidence) of
these procedures.
(3) As set forth in subsections 8(a) and
(b) (Determination Process) of these
procedures, CITA will determine
whether the subject product of the
Request to Remove or Restrict is
available in commercial quantities
in a timely manner in the DRCAFTA countries not later than 30
U.S. business days after the official
receipt of the request.
(i) If CITA determines that the product
is available in commercial
quantities in a timely manner in the
DR-CAFTA countries, e.g., that a
CAFTA-DR supplier is capable to
supply the entire subject product
requested originally, then that
product will be removed from the
Commercial Availability List in
Annex 3.25 of the Agreement.
(ii) If CITA determines that the
product is available in restricted
quantities in a timely manner in the
CAFTA-DR countries, e.g., that a
CAFTA-DR supplier is capable to
supply part of the subject product
requested originally then a
restricted quantity will be
introduced for that product.
(iii) If the Commercial Availability
List changes as a result of CITA’s
determination for the Request to
Remove or Restrict, CITA will
notify interested parties by email of
its determination and will publish a
notice of its determination for the
request to remove or restrict in the
U.S. Federal Register.
(A) For removal, the notice will state
PO 00000
Frm 00029
Fmt 4703
Sfmt 4703
that textile and apparel articles
containing the subject product are
not to be treated as originating in a
CAFTA-DR country if the subject
product is obtained from nonCAFTA-DR sources, effective for
goods entered into the United States
on or after six months (i.e., 180
calendar days) after the date of
publication of the notice.
(B) For restriction, the notice will
specify the restricted quantity for
the subject product that is to be
effective on or after six months (i.e.,
180 calendar days) after the
publication date of the notice.
R. Matthew Priest,
Chairman, Committee for the Implementation
of Textile Agreements.
[FR Doc. E7–5102 Filed 3–20–07; 8:45 am]
BILLING CODE 3510–DS–S
DEPARTMENT OF EDUCATION
Office of Special Education and
Rehabilitative Services; Overview
Information; Centers for Independent
Living; Notice Inviting Applications for
New Awards for Fiscal Year (FY) 2007
Catalog of Federal Domestic Assistance
(CFDA) Number: 84.132A.
Dates: Applications Available: March
21, 2007.
Deadline for Transmittal of
Applications: April 20, 2007.
Deadline for Intergovernmental
Review: June 19, 2007.
Eligible Applicants: To be eligible to
apply, an applicant must—
(a) Be a consumer-controlled,
community-based, cross-disability,
nonresidential, private nonprofit
agency;
(b) Have the power and authority to—
(1) carry out the purpose of part C of
title VII of the Rehabilitation Act of
1973, as amended (the Act) and perform
the functions listed in section 725(b)
and (c) of the Act and subparts F and
G of 34 CFR part 366 within a
community located within a State or in
a bordering State; and
(2) Receive and administer—
(i) Funds under 34 CFR part 366;
(ii) Funds and contributions from
private or public sources that may be
used in support of a center for
independent living (center); and
(iii) Funds from other public and
private programs;
(c) Be able to plan, conduct,
administer, and evaluate a center
consistent with the standards and
assurances in section 725(b) and (c) of
the Act and subparts F and G of 34 CFR
part 366;
E:\FR\FM\21MRN1.SGM
21MRN1
Agencies
[Federal Register Volume 72, Number 54 (Wednesday, March 21, 2007)]
[Notices]
[Pages 13256-13264]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-5102]
=======================================================================
-----------------------------------------------------------------------
COMMITTEE FOR THE IMPLEMENTATION OF TEXTILE AGREEMENTS
Final Procedures for Considering Requests Under the Commercial
Availability Provision of the Dominican Republic-Central America-United
States Free Trade Agreement
March 15, 2007.
AGENCY: Committee for the Implementation of Textile Agreements (CITA).
ACTION: Summary and response to comments concerning the CAFTA-DR
commercial availability interim procedures; notice of final procedures.
-----------------------------------------------------------------------
SUMMARY: This notice summarizes the comments received concerning the
Interim Procedures and provides responses to those comments. See
Interim Procedures for Considering Requests Under the Commercial
Availability Provision to the Dominican Republic-Central America-United
States Free Trade Agreement, 71 FR 9315 (February 23, 2006).
EFFECTIVE DATE: The date of entry into force of the Dominican-Central
America-United States Free Trade Agreement.
FOR FURTHER INFORMATION CONTACT: Richard Stetson, Office of Textiles
and Apparel, U.S. Department of Commerce, (202) 482-3400.
SUPPLEMENTARY INFORMATION:
Authority: Section 203(o)(4) of the Dominican Republic-Central
America-United States Free Trade Agreement Implementation Act
(``CAFTA-DR''); the Statement of Administrative Action (``SAA''),
accompanying the CAFTA-DR, at 16-20.
Comments and Responses Concerning the Interim Procedures
On February 21, 2006, the Committee for the Implementation of
Textile Agreements (``CITA'') issued a Federal Register notice advising
interested parties of Interim Procedures that CITA would follow in
implementing certain provisions of the Dominican Republic-Central
America-United States Free Trade Agreement Implementation Act (``CAFTA-
DR Implementation Act''), namely the procedures for modification of the
list of fabrics, yarns or fibers not available in commercial quantities
in a timely manner in the countries that are Parties to the CAFTA-DR
Agreement (``CAFTA-DR'' or ``Agreement''), as set out in Annex 3.25 of
the CAFTA-DR. CITA has reviewed and considered all submitted comments,
and below is a summary of and response to those comments.
Standards For Submissions: One commentator noted that the interim
procedures did not provide a factual standard for determining the
substitutability of other products for the product subject to the
commercial availability request. See, e.g., sections 4(b)(4) and
6(b)(2)(iv) of the Interim Procedures. CITA has not adopted this
suggestion. A wide range of products may be the subject of a commercial
availability request. As each commercial availability request is
evaluated on the basis of the facts contained therein, it would be
impracticable to set forth a uniform standard for substitutability;
[[Page 13257]]
rather, CITA will examine each request and any subsequent responses on
a case-by-case basis.
The same commentator suggested that an offer made in response to a
request must contain an explicit commitment by the potential CAFTA-DR
supplier to immediately deliver the product in question or one
determined to be substitutable. CITA has not adopted this suggestion.
Section 203(o)(4)(C) of the CAFTA-DR Implementation Act sets forth the
standard that the subject product be delivered ``in a timely manner.''
What is ``timely'' in any given situation can only be determined on a
case-by-case basis.
One commentator asked that CITA clarify that in addition to
accepting responses that object to a request, CITA will also accept
submissions in support of a request. Section 203(o)(4)(C)(iii)(II) of
the CAFTA-DR Implementation Act provides for a determination as to
whether any ``interested entity has objected to the request.'' Section
6 of the Interim Procedures required that an objection to the request
contain an offer to supply, and that both offers to supply and rebuttal
submissions provide information to substantiate the claims contained in
the respective submissions. This requirement is maintained in section 6
of the Final Procedures. Thus, CITA will not consider submissions in
support of a request in making commercial availability determinations.
Removal From Annex 3.25 List: One commentator noted that the
procedures should contain an explicit statement that all products
already approved under Trade Preference Programs (Caribbean Basin Trade
partnership Act (``CBTPA''), African Growth and Opportunity Act
(``AGOA''), and the Andean Trade Promotion and Drug Eradication Act
(``ATPDEA'') and added to the list in Annex 3.25 of CAFTA-DR cannot be
removed from Annex 3.25. A different commentator asked that CITA
confirm that products added to the list in Annex 3.25 since the date
that the CAFTA-DR was signed cannot be removed from that list. Article
3.25.5(a) of the CAFTA-DR and section 203(o)(4)(E)(I) of the CAFTA-DR
Implementation Act provide that fabrics, yarns, or fibers added to the
list in Annex 3.25 since the date the CAFTA-DR was signed are subject
to removal. Section 9 of Final Procedures accurately reflects these
statutory requirements.
Public Notice: One commentator asserted that the procedures'
reliance on Internet notification and electronic mail (``email'')
correspondence will result in delays or failures to distribute the
information fully, especially for small companies relying on outside
consultants. Moreover, the commentator stated that forbearing the use
of a Federal Register notification results in greater risk for parties
to be uninformed of developments in these proceedings. Another
commentator alleges that as these procedures are a federal
administrative process, publication in the Federal Register is required
so that all parties may be assured of notification. Given the
abbreviated timeline for these proceedings, Internet and email
communications provide more timely notification than publication in the
Federal Register and allow all parties equal opportunity for
notification. This is particularly relevant for parties outside of the
United States. Further, given the abbreviated timeline for such
proceedings, Internet and email communications provide interested
entities with more time to allocate to reviewing information and
providing submissions than Federal Register publication would allow.
Moreover, although a notice published in the Federal Register does
constitute ``public notice,'' it is not the only means by which to
notify the public. CITA has widely publicized that any interested party
may receive its email notifications and that all public documents will
be posted on its website. This system provides broad access and
accessibility to interested parties inside and outside of the United
States.
Another commentator noted that CITA's requirement to submit hard
copies of submissions via express courier is too inflexible, and
requests that CITA accept hand-delivered submissions accompanied by an
appropriate receipt that allows confirmation of delivery. CITA has not
adopted this suggestion. In light of the abbreviated timeline for such
proceedings, delivery by express courier permits tracking of
submissions and avoids the possibility of documents being lost or
misplaced.
One commentator asked that CITA accept submissions of electronic
information in PDF format. CITA has adopted this suggestion and
clarified this point in the Final Procedures.
Other commentators asked that CITA advise interested parties of all
deadlines, extensions, availability of samples for public inspection,
and the posting of responses on the website in its email notifications.
Additional commentators requested that the procedures clarify that
information on determinations, including ``Deemed Approvals'' and
removal of restrictions will be provided through email notifications,
website postings, and publication in the Federal Register. CITA has
adopted this suggestion and clarified these points in its Final
Procedures.
Contents of Requests and Responses: A commentator suggested that
requests should include ``offers to buy,'' as responses are required to
contain ``offers to supply,'' to prevent speculative and spurious
requests by potential buyers. CITA has not adopted this suggestion.
CITA has no authority to obligate or compel requesters to purchase
products, and therefore, cannot require requesters to include an
``offer to buy.'' However, should a subject or substitutable product be
available from a CAFTA-DR supplier, articles containing such products
from third-country sources would not qualify for preferential trade
benefits.
Another commentator suggested that denials, approvals in restricted
quantities, or removals contain contact information of the potential
CAFTA-DR supplier(s) of the subject product(s). This information would
already be contained in any response with an offer to supply or
rebuttal submission. Moreover, as this information is posted on the
Internet, there is no need to duplicate such information in CITA's
determination notice.
The same commentators suggested that responses with an offer to
supply should contain a sample of the petitioned or allegedly
substitutable product. CITA is not adopting this suggestion. CITA notes
that given the abbreviated timeline to conduct these proceedings and
depending on the nature of the requested product, it may not be
possible for an interested entity to provide a sample in all
situations. Samples may be submitted with requests or offers to supply,
but this is not required. CITA notes that in the event that the 14-day
extension is invoked, interested entities are provided with additional
time to provide a sample product to substantiate their claims should
they choose to do so.
A commentator asked that CITA allow discretion regarding treatment
of business confidential information in special circumstances, such as
when a potential supplier wants to keep its name confidential for fear
of retaliation. CITA has not adopted this suggestion. In order to
conduct this procedure in an open and fair manner, CITA finds it is
necessary for all participants to know: (1) the names of potential
suppliers that have been contacted by petitioners, and (2) those
interested entities who object to the request. However, specific
proprietary information may be treated as business confidential
information. See section 3 of the Final Procedures.
[[Page 13258]]
Restricted Quantities: One commentator was strongly opposed to an
automatic review of restricted quantities in a CITA determination,
alleging that such reviews would burden parties and CITA with
unnecessary processes. Moreover, this commentator claims that the
automatic review is not required by the legislation. Section
203(o)(4)(C)(vi) of the CAFTA-DR Implementation Act provides that the
restriction may be eliminated not later than six months after the
product is added to the list in Annex 3.25 of the Agreement in a
restricted quantity. Therefore, CITA may review current circumstances
to determine whether eliminating the restricted quantity is warranted.
This section of the Final Procedures has been revised to provide
clarity. See section 8(c)(3) of the Final Procedures.
One commentator asked that CITA specify how it will determine a
given quantity in determinations that involve restricted quantities. In
the course of the proceeding, based on the information submitted , CITA
will specify an amount that can be provided by the CAFTA-DR
supplier(s). CITA will provide additional explanation in a Frequently
Asked Questions (``FAQ'') document that will be made available on its
website.
Another commentator requests that in section 8(c)(2) of the Interim
Procedures, regarding approvals in unrestricted quantities, the
language be modified to read, ``... if CITA determines that no CAFTA-DR
supplier(s) or manufacturer(s) could fulfill any amount of the
request.'' CITA has determined to remove this sentence all together, as
it is redundant to the previous sentence.
The same commentator asked that CITA consider eliminating a
quantity restriction only upon receipt of a request from an interested
entity. CITA has not adopted this suggestion. Section 203(o)(4)(C)(vi)
of the CAFTA-DR Implementation Act does not require that a request be
submitted to CITA, but only that CITA may remove the restriction within
six months after the product is added to the Annex 3.25 list in a
restricted quantity.
A commentator asked that CITA clarify that approvals in restricted
quantities take effect 30 days after the official receipt of the
request. CITA is required to make a determination, whether a denial,
approval in an unrestricted quantity, or an approval in a restricted
quantity, within the 30 U.S. business-day deadline, with the caveat
that CITA may extend the deadline for an additional 14 U.S. business
days should additional information be required. See Section 8(c) of the
Interim and Final Procedures.
Another commentator asked that CITA specify that the effective date
of the elimination of a restriction will be six months after the date
of publication of the notice. CITA has not adopted this suggestion.
CITA notes that section 203(o)(4)(C)(vi) of the CAFTA-DR Implementation
Act does not specify the effective date for removal of the restricted
quantity should CITA make such a determination. CITA would publish in
the Federal Register any modification to products on the Annex 3.25
list, such as removal of a restriction, which in effect adds a product
to the Annex 3.25 list in an unrestricted quantity. CITA notes that
section 203(o)(4)(C)(v) of the CAFTA-DR Implementation Act specifies
that the effective date for adding products to the Annex 3.25 list in
an unrestricted or restricted quantity is the date of publication in
the Federal Register.
A commentator asked that CITA clarify that a review to determine
whether to remove restricted quantities can take place later than six
months after adding the product in a restricted quantity to the Annex
3.25 list. CITA has not adopted this suggestion. The procedure in
section 8(c)(3)(ii) of the Final Procedures implements Section
203(o)(4)(C)(vi) of the CAFTA-DR Implementation Act which provides only
for a review not later than six months after the product is added to
the Annex 3.25 list in a restricted quantity.
Changed Circumstances: Several commentators requested that CITA
clarify a discrepancy in the timeframes provided for reconsideration of
determinations in sections 8(c)(6) and 9(a) of the interim procedures.
Another commenter requested that CITA strike section 8(c)(6).
In section 8(c)(6) of the Interim Procedures, CITA proposed to
allow for proceedings based upon changed circumstances. Several
commentators expressed that CITA does not possess statutory authority
to conduct changed circumstances proceedings. The Final Procedures
clarify when it is appropriate for the agency to conduct a proceeding
based upon changed circumstances. It is CITA's intention at this time
to exercise its inherent authority to reconsider, and/or subsequently
amend, commercial availability determinations that may have been
procured by, e.g., error, fraud, or similar faults. See, e.g., Elkem
Metals, et al. v. United States, 26 C.I.T. 234, 239, 193 F. Supp. 2d
1314, 1319-20 (2002) (``It is indeed the general rule that
administrative agencies in general...have the inherent authority to
institute reconsideration proceedings so as to `vindicate the integrity
of the administrative process.'''); Belville Min. Co. v. U.S., 999 F.2d
989, 997 (6th Cir. 1993) (``Even where there is no express
reconsideration authority for an agency...the general rule is that an
agency has inherent authority to reconsider its decision, provided that
reconsideration occurs within a reasonable time after the first
decision.'')(citations and internal quotations omitted)); Bookman v.
United States, 197 Ct. Cl. 108, 453 F.2d 1263, 1265 (1972) (explaining
the general rule that ``every tribunal, judicial or administrative, has
some power to correct its own errors or otherwise modify its judgment,
decree, or order'' and that ``[courts] will sustain the reconsidered
decision of an agency, as long as the administrative action is
conducted within a short and reasonable time'') (citations and internal
quotations omitted)); Gilmore Steel Corp. v. U.S., 7 C.I.T. 219, 223,
585 F. Supp. 670, 674 (1984) (holding that the International Trade
Administration had the authority to correct a manifest error that
``taints the proceeding''); Gun South, Inc. v. Brady, 877 F.2d 858, 862
(11th Cir. 1989) (concluding that the Bureau of Alcohol, Tobacco, and
Firearms ``must necessarily retain the power to correct the erroneous
approval of firearms import applications'' despite the absence of
express statutory authority).
Therefore, the proposed changed circumstances provision was not
based on statutory changes made by the CAFTA-DR Implementation Act, but
rather relied on the longstanding inherent authority that CITA has
always possessed. See cases cited supra. Further, neither the CAFTA-DR
Implementation Act nor case precedent prohibits the proposed
proceeding. In the interest of fairness and transparency, however, it
seems appropriate to clarify the agency's inherent authority to address
such faults in the conduct of the proceeding. In the Final Procedures,
CITA has deleted section 8(c)(6) and provided a clarification in the
``Background'' section.
Deadlines: Several commentators noted that the deadlines set forth
by the procedures do not allow for extensions for responses with offers
to supply or rebuttal comments. The procedures do allow for CITA to
extend the time limit for responses with offers to supply and rebuttal
comments. However, even if an extension is provided, CITA is required
to meet the statutory deadline for making a determination. See sections
6 and 7of the Final Procedures; see also,
[[Page 13259]]
e.g., section 203(o)(4)(C)(iv) of the CAFTA-DR Implementation Act.
Another commentator suggested that CITA begin the timeline for the
proceeding from the date of publication of the commercial availability
request rather than the date of its official receipt by CITA, which
would allow for two additional days for submitting responses with
offers to supply. CITA has not adopted this suggestion, as CITA needs
sufficient time to review the completeness of commercial availability
requests before notifying interested parties that a commercial
availability request has been submitted and accepted. At the same time,
the statute requires that the determination be made within a certain
time period from the date of submission. Therefore, in order for CITA
to make a commercial availability determination within the statutorily
prescribed deadlines, CITA needs the two days in question to review the
completeness of the commercial availability request before notifying
interested parties that a request has been submitted and accepted. See
section 203(o)(4)(C)(iv) of the CAFTA-DR Implementation Act.
Another commentator suggested that when CITA seeks to meet with
interested entities during an extended review period, the meeting
should include all sides of the issue and be open to the public. Should
CITA convene a meeting between the requester and interested entities
providing offers to supply, such meetings will be public and conducted
in an open manner.
A commentator explained that the procedures should state that CITA
may determine to extend the 30-day deadline for an additional 14 days
to obtain additional information. Section 8 of the Final Procedures
explains that CITA is permitted to extend the 30 U.S. business-day
deadline for an additional 14 U.S. business days. This same section of
the procedures clearly explains the purpose of the 14 U.S. business day
extension. See also section 203(o)(4)(c)(iv) of the CAFTA-DR
Implementation Act.
Another commentator asked that CITA add in section 8(c)(3)(i) of
the Interim Procedures the phrase, ``or not more than 44 U.S. business
days where extension is provided...'' CITA has adopted this suggestion
in its Final Procedures.
A commentator requested that CITA clarify that if CITA provides an
extension for submitting responses with offers to supply, CITA's
determinations will still meet the statutory deadline. CITA has adopted
this suggestion in its Final Procedures.
One commentator asked that CITA acknowledge that in ``emergency
circumstances'' CITA could make a decision prior to its 30 U.S.
business-day deadline. CITA has not adopted this suggestion. CITA is
required to make a determination ``within'' 30 U.S. business days of
receipt of a commercial availability request, unless an extension is
provided. See section 203(o)(4)(C)(iv) of the CAFTA-DR Implementation
Act. Moreover, each proceeding must allow all interested entities
sufficient time to respond with offers to supply and provide rebuttal
comments in the course of the proceeding.
Deemed Approval: One commentator objected to the provision
regarding ``Deemed Approval,'' noting that such requirements set a
negative precedent for future procedures. CITA has not adopted this
suggestion. Section 203(o)(4)(D) of the CAFTA-DR Implementation Act
provides expressly for the ``Deemed Approval'' procedure.
Another commentator asked that the ``Deemed Approval'' provision
apply to all determinations in these proceedings, not only to
commercial availability requests to add a given product to Annex 3.25.
Section 203(o)(4)(D) of the CAFTA-DR Implementation Act provides that
the ``Deemed Approval'' process only applies to commercial availability
requests and not to requests to remove or restrict.
Interested Entities: One commentator claimed that CITA
inadvertently limited participation in commercial availability
proceedings by using the term ``interested entities'' to identify who
may request to be included on the email notification list. The Final
Procedures clarify that any interested party can be included on the
mass email notification list.
Another commentator asked that CITA clarify that trade associations
are an ``interested entity.'' CITA has not adopted this suggestion. The
term ``interested entity'' is defined in section 203(o)(4)(B)(i) of the
CAFTA-DR Implementation Act, and this definition does not include trade
associations. However, trade associations can participate in the
process as an interested party.
A commentator noted that the language of the procedures differs
from the Agreement and the CAFTA-DR Implementation Act, using the
standard for determining whether to add a product to the Annex 3.25
list as ``are not available'' instead of ``are available'' in the
CAFTA-DR countries. The language of the procedures is consistent with
both the Agreement and the CAFTA-DR Implementation Act.
One commentator asked that CITA clarify that non-essential
character components are eligible for determinations. The CAFTA-DR
Implementation Act provides for determinations whether ``fabrics,
yarns, or fibers'' are to be added to the list in Annex 3.25 of the
Agreement. See section 203(o)(4)(A). Further, Section Notes 2, 3, and 4
to Section XI of Annex 4.1 of the Agreement provides for how the list
of fabrics, yarns, and fibers in Annex 3.25 is taken into account in
applying the Agreement's rules of origin. Nothing in the commercial
availability process alters the rules of origin contained in the
Agreement.
Several commentators asked that CITA elaborate on several of the
provisions included in the procedures, including ``Deemed Approval,''
approvals with restricted quantities, the contents of commercial
availability requests, responses with offers to supply, and rebuttal
comments. CITA has adopted this suggestion and will provide further
explanations in a FAQ document to be made available on its website.
Another commentator asked that CITA review its procedures after one
year to determine if any modifications are necessary. The Final
Procedures provide that the procedures may be modified at any time to
address concerns that may arise. CITA notes that these are
administrative procedures rather than regulations, and can be modified
as needed.
Final Procedures
This notice also sets forth the final procedures the Committee for
the Implementation of Textile Agreements (``CITA'') will follow in
implementing certain provisions of the Dominican Republic-Central
America-United States Free Trade Agreement Implementation Act (``CAFTA-
DR Implementation Act''). Section 203(o)(4) of the CAFTA-DR
Implementation Act establishes procedures for the President to modify
the list of fabrics, yarns, or fibers not available in commercial
quantities in a timely manner in the countries that are Parties to the
CAFTA-DR, as set out in Annex 3.25 of the Agreement. The President has
delegated to CITA the authority to determine whether a fabric, yarn, or
fiber is not available in commercial quantities in a timely manner in
CAFTA-DR countries and has directed CITA to establish procedures that
govern the submission of a request and provide the opportunity for
interested entities to submit comments and supporting evidence in any
such determination pursuant to the CAFTA-DR Implementation Act. This
notice
[[Page 13260]]
hereby gives notice to interested parties of the procedures CITA will
follow in considering such requests.
Background:
The CAFTA-DR provides a list in Annex 3.25 of the Agreement for
fabrics, yarns, and fibers that the Parties to the Agreement have
determined are not available in commercial quantities in a timely
manner from suppliers in the United States or other CAFTA-DR countries.
A textile and apparel good containing fabrics, yarns, or fibers that is
included in Annex 3.25 of the Agreement may be treated as if it is an
originating good for purposes of the specific rules of origin in Annex
4.1 of the Agreement, regardless of the actual origin of those inputs,
provided that all other fabrics, yarns, or fibers of the component that
determines the classification of the good meet the specific rules of
origin in Annex 4.1 of the Agreement. The CAFTA-DR Implementation Act
provides that the President will establish procedures governing the
submission of requests and may determine whether additional fabrics,
yarns, or fibers are not available in commercial quantities in a timely
manner in the United States or the other CAFTA-DR countries. In
addition, the CAFTA-DR Implementation Act establishes that the
President may remove a fabric, yarn, or fiber from the list, if it has
been added to the list in an unrestricted quantity pursuant to section
203(o), if he determines that the fabric, yarn, or fiber has become
available in commercial quantities in a timely manner.
The SAA provides that the President will delegate to CITA his
authority under section 203(o)(4) of the Agreement (``Commercial
Availability Provision''), to establish procedures for modifying the
list of fabrics, yarns, or fibers not available in commercial
quantities in a timely manner for Agreement countries, as set out in
Annex 3.25 of the Agreement.
These procedures are not subject to the requirement to provide
prior notice and opportunity for public comment, pursuant to 5 U.S.C.
553(b)(A) (Administrative Procedures Act). These procedures may be
modified in the future to address concerns that may arise as CITA gains
experience in implementing them. CITA possesses inherent authority to
reconsider, and/or subsequently amend, commercial availability
determinations that may have been procured by error, fraud, or similar
faults. Should CITA undertake to review a determination under such
circumstances, CITA will provide notice to the public, through the
email and website notification processes described in the Final
Procedures, and provide opportunity for interested entities to submit
comments and information for CITA's consideration.
Procedures for Considering Requests
1. Introduction
The intent of the CAFTA-DR Commercial Availability Procedures is to
foster the use of U.S. and CAFTA-DR products by implementing procedures
that allow products to be placed on or removed from a product list, on
a timely basis, and in a manner that is consistent with normal business
practice. To this end, these procedures are intended to facilitate the
transmission, on a timely basis, of order requests and offers to supply
such requests; have the market indicate the availability of the supply
of products that are the subject of requests; make available promptly,
to interested entities and parties, information regarding the requests
for products and offers to supply received; ensure wide participation
by interested entities and parties; provide careful scrutiny of
information provided to substantiate order requests and response to
supply offers; and provide timely public dissemination of information
used by CITA in making commercial availability determinations.
2. Definitions
(a) Commercial Availability Request. A ``Commercial Availability
Request'' is a submission from an interested entity requesting that
CITA place a good on the list in Annex 3.25 because that fiber, yarn,
or fabric is not available in commercial quantities in a timely manner
from a supplier in the CAFTA-DR countries.
(b) Interested Entity. An ``interested entity'' means a government that
is a Party to the Agreement, other than the United States; a potential
or actual purchaser of a textile or apparel good; or a potential or
actual supplier of a textile or apparel good. CITA recognizes that a
legal or other representative may act on behalf of an `interested
entity.' See section 203(o)(4)(B)(i) of the CAFTA-DR Implementation
Act.
(c) Interested Party. An ``interested party'' means any interested
person that requests to be included on the email notification list for
Commercial Availability proceedings. Any interested person may become
an interested party by contacting CITA. See Office of Textile and
Apparel, U.S. Department of Commerce, website for details at https://
web.ita.doc.gov/tacgi/CABroadcast.nsf/Document?Openform or send an
email to OTEXACAFTA@ita.doc.gov.
(d) Official Receipt. The ``official receipt'' is CITA's email
confirmation that it has received both the email version and the
original submission signed by the interested entity delivered via
express courier.
(e) Request. A ``request'' refers to the Commercial Availability
Request.
(f) Request to Remove or Restrict. A ``request to remove or restrict''
is a submission from an interested entity, made no sooner than six
months after a product has been added to the Annex 3.25 list in an
unrestricted quantity pursuant to Section 203(o) of the CAFTA-DR
Implementation Act, requesting that CITA either remove a product or
that a quantity restriction be introduced.
(g) Requestor. The ``requestor'' refers to the interested entity that
files a request, either a Commercial Availability Request or a Request
to Remove or Restrict, under the CAFTA-DR Commercial Availability
provision, for CITA's consideration.
(h) CAFTA-DR Supplier. A ``CAFTA-DR supplier'' is a potential or actual
supplier of a textile or apparel good in the territory of any Party.
(i) Response with an Offer. A ``response with an offer'' is a
submission from an interested entity to CITA providing its objection to
the request or asserting its ability to supply the subject product by
providing an offer to supply the subject product described in the
request.
(j) Rebuttal Comment. A ``rebuttal comment'' is a submission from an
interested entity providing information in response to evidence or
arguments raised in a response with an offer submission. Rebuttal
comments must be limited to evidence and arguments provided in a
response with an offer submission.
(k) Fiber, Yarn, or Fabric. The term ``fiber, yarn, or fabric'' means a
single product or a range of products, which meet the same
specifications provided in a submission, and which may be only part of
a Harmonized Tariff Schedule of the United States (``HTSUS'')
provision.
(l) U.S. Business Day. A ``U.S. business-day'' is any calendar day
other than a Saturday, Sunday, or a legal holiday. See section
203(o)(4)(B)(i) of the CAFTA-DR Implementation Act.
3. Submissions for Participation the CAFTA-DR Commercial Availability
Proceeding.
(a) Filing a Submission.All submissions for a CAFTA-DR Commercial
Availability proceeding (e.g., Commercial Availability Request,
Response with an Offer, Rebuttal Comments, and Request to Remove or
Restrict) must be in English. If any
[[Page 13261]]
attachments are in a language other than English, then a translation
must be provided. Each submission must be submitted to the U.S.
Department of Commerce's Office of Textiles and Apparel (``OTEXA'') in
two forms, electronic mail and original signed submission.
(1) An electronic mail (``email'') version of the submission must be
either in PDF, Word, or Word-Perfect format and must contain an
adequate public summary of any business confidential information and
the due diligence certification, sent to OTEXA--CAFTA@ita.doc.gov. The
``email'' version of the submission will be posted for public review on
OTEXA's CAFTA-DR Commercial Availability website at
http:otexa.ita.doc.gov. No business proprietary information should be
submitted in the ``email'' version of any document.
(2) The original signed submission must be received via express courier
to--Chairman, Committee for the Implementation of Textile Agreements,
Room H3100, U.S. Department of Commerce, 14th and Constitution Ave.,
N.W., Washington, DC 20230. Any business confidential information upon
which an interested entity wishes to rely must be included in the
original signed submission only. Except for the inclusion of business
confidential information, the two versions of a submission should be
identical.
(3) Brackets must be placed around all business confidential
information contained in submissions. Documents containing business
confidential information must have a bolded heading stating
``Confidential Version.'' Attachments considered business confidential
information must have a heading stating ``Business Confidential
Information.'' Documents, including those submitted via ``email,''
provided for public release, must have a bolded heading stating
``Public Version'' and all the business confidential information must
be deleted and substituted with asterisks.
(4) Generally, details, such as quantities and lead times for providing
the subject product, can be treated as business confidential
information. However, the names of suppliers who were contacted, what
was asked generally about the capability to manufacture the subject
product, and the responses thereto should be included in public
versions, which will be made available to the public.
(b) Due Diligence Certification. An interested entity must file a
certification of due diligence as described in subsection (b)(1) with
each submission, both email and original signed versions, containing
factual information. If the interested entity has legal counsel or
other representative, the legal counsel or other representative must
file a certification of due diligence as described in subsection (b)(2)
with each submission, both email and original signed versions,
containing factual information. Accurate representations of material
facts submitted to CITA for the CAFTA-DR Commercial Availability
proceeding are vital to the integrity of this process and are necessary
for CITA's effective administration of the statutory scheme. Each
submission containing factual information for CITA's consideration must
be accompanied by the appropriate certification regarding the accuracy
of the factual information. Any submission that lacks the applicable
certifications will be considered an incomplete submission that CITA
will reject and return to the submitter. CITA may verify any factual
information submitted by interested entities in a CAFTA-DR Commercial
Availability proceeding.
(1) For the person responsible for presentation of the factual
information: I, (name and title), currently employed by (interested
entity), certify that (1) I have read the attached submission, and (2)
the information contained in this submission is, to the best of my
knowledge, complete and accurate.
(2) For the person's legal counsel or other representative:I, (name),
of (law or other firm), counsel or representative to (interested
entity), certify that (1) I have read the attached submission, and (2)
based on the information made available to me by (person), I have no
reason to believe that this submission contains any material
misrepresentation or omission of fact.
(c) Official Receipt. A submission will be considered officially
submitted to CITA only when both the email version and the original
signed submission have been received by CITA. For request submissions,
CITA will confirm to the requestor that both versions of the request
submission were received through an email confirmation. CITA's email
confirmation shall be considered the ``official receipt'' of the
request submission, and also begins the statutory 30 U.S. business-day
process for CITA consideration of requests. CITA will confirm official
receipt of response and rebuttal submissions by posting the response or
rebuttal on the dedicated website at https://web.ita.doc.gov/tacgi/
CaftaReqTrack.nsf.
4. Submitting a Request for Consideration in a Commercial Availability
Proceeding.
(a) Commercial Availability Request. An interested entity may submit a
Commercial Availability request to CITA alleging that a fiber, yarn, or
fabric is not available in commercial quantities in a timely manner
from a producer in the CAFTA-DR countries.
(b) Contents of a Commercial Availability Request.
(1) Detailed Product Information. The Commercial Availability request
must provide a detailed description of the product subject to the
request, including, if applicable, fiber content, construction, yarn
size, and finishing processes; and the classification of the product
under the HTSUS. All measurements in the entire submission must be
stated in metric units, or if the English count system is used in any
part, then a conversion to metric units must be provided.
(2) Quantity. The Commercial Availability request must provide the
specific quantity of the product needed by the requestor, in standard
units of quantity for production of the subject product in the CAFTA-DR
countries.
3) Due Diligence. The Commercial Availability request must provide a
complete description of the due diligence undertaken by the requestor
to determine the subject product's availability in the CAFTA-DR
countries. Due diligence for the requestor means it has made reasonable
efforts to obtain the subject product from CAFTA-DR suppliers. The
requestor must provide the names and addresses of suppliers contacted,
who was specifically contacted, the exact request that was made, the
dates of those contacts, whether a sample of the subject product was
provided for review, and the exact response given for the supplier's
inability to supply the subject product under the same conditions as
contained in the Commercial Availability request submitted to CITA, in
addition to any other information the requestor believes is relevant.
The requestor must submit copies or notes of relevant correspondence,
both inquiries and responses, with these
[[Page 13262]]
suppliers. Relevant correspondence includes notes of telephone
conversations. Specific details of correspondence with suppliers, such
as quantities and lead times for providing the subject product, can be
treated as business confidential information. However, the names of
CAFTA-DR suppliers who were contacted, what was asked generally about
the capability to manufacture the subject product, and the responses
thereto should be available for public review to ensure proper public
participation in the process. ``Lead times'' refers to supplying the
subject product within normal business time frames for the subject
product once an order is received. Specific delivery dates are not
necessary. Required delivery dates that fall within the time needed to
complete the Commercial Availability determination process are not
acceptable.
(4) Substitutable Products. The Commercial Availability request must
provide information on whether the requester believes that other
products supplied by the CAFTA-DR supplier are not substitutable in
commercial quantities in a timely manner for the product(s) that is
(are) the subject of the request for purposes of the intended use.
Clearly describe the unique characteristics of the subject product that
distinguishes it from other similar or potentially substitutable
products. Describe why such characteristics are required for the
purposes of the end-use of the product and cannot be substituted by
another product available from a CAFTA-DR supplier.
(5) Additional Information. The Commercial Availability request may
provide any additional evidence or information believed to be relevant
for CITA to determine whether a fiber, yarn, or fabric is not available
in commercial quantities in a timely manner from a producer in the
CAFTA-DR countries.
5. Consideration and Acceptance of a Request.
In considering whether to accept a request, CITA will consider and
determine whether it provides all the required information specified in
sections 3 and 4 of these procedures. CITA will determine whether to
accept the request for consideration and investigation not later than
two U.S. business days after the official receipt of a request.
(a) Request Rejected. If CITA determines that the request does not
contain the required information, the requestor will be notified
promptly by email that the request has not been accepted and the
reasons for the rejection. A request may be resubmitted with additional
information for the subject product and CITA will reevaluate it as a
new request.
(b) Request Accepted. If CITA determines that the request contains the
required information, CITA will notify interested parties by email that
a request has been accepted and filed and will assign a File Number.
CITA will post the accepted request on its website for public notice.
The email notification and the website posting will indicate the
calendar date deadlines for submitting offers to supply and submitting
rebuttal responses.
6. Submitting a Response with an Offer in a Commercial Availability
Proceeding.
Respondents must meet the requirements outlined in 3 of these
procedures. General comments in support of or opposition to a
commercial availability request do not meet the requirements of a
Response with an Offer. A Due Diligence Certification must accompany a
Response with an Offer.
(a) Response With an Offer Submission. An interested entity may file a
response submission to a request CITA accepted advising CITA of its
objection to the request and its ability to supply the subject product
by providing an offer to supply the subject product as described in the
request. An interested entity will have 10 U.S. business days after
official receipt of a request to respond to a request. If good cause is
shown, CITA may extend this deadline, but CITA will still meet the
statutory deadline for making a determination.
(b) Contents of a Response with an Offer.
(1) File Number. The Response with an Offer needs to reference the CITA
File Number assigned to the particular Commercial Availability Request
being addressed.
(2) Quantity. The Response with an Offer must supply the quantity of
the requested subject product that the CAFTA-DR supplier, is capable of
currently supplying, in standard units of quantity. All measurements
must be in metric units. If the English count system is used in any
part, then a conversion to metric units must be provided.
(3) Production Capability. The Response with an Offer must report the
quantity, in metric units, that the CAFTA-DR supplier produced of the
subject product, or a substitutable product, in the preceding 24-month
period.
(i) For products that have experienced cyclical demand or are not
currently produced, the CAFTA-DR supplier should indicate the quantity
that has been supplied or offered commercially in the past, with an
explanation of the reasons it is not currently produced or offered.
(ii) If the requestor has requested a new style, weight, or other
variation that is new to the market or new to the respondent, then the
CAFTA-DR supplier(s) should provide detailed information on its current
ability to make the subject product.
(iii) If the CAFTA-DR supplier(s) are making a new product that has
not yet been offered to the market, but could meet the requirements of
the subject product, then the CAFTA-DR supplier(s) need(s) to provide
detailed information regarding the product and their ability to meet a
request.
(iv) Substitutable Products. The Response with an Offer may
provide, if relevant, the basis for the responder's belief that other
products that are supplied by the CAFTA-DR supplier in commercial
quantities in a timely manner are substitutable for the product(s) that
are the subject of the request for purposes of the intended use.
(4) Due Diligence. The Response with an Offer must provide a complete
description of the due diligence undertaken by the CAFTA-DR supplier to
substantiate the ability to supply the subject product.
(i) In the case of new variations of a product, the CAFTA-DR
supplier must substantiate the ability to manufacture the subject
product. The CAFTA-DR supplier must provide sufficient detail of the
manufacturing capabilities of the facility that will supply the subject
product, in addition to any other information the supplier believes is
relevant.
(ii) If some operations, such as finishing, will be completed by
other entities, the name of the facility and contact information must
be provided.
(5) Location of the CAFTA-DR supplier. The Response with an Offer must
provide the name, address, phone number, and email address of a contact
person at the facility claimed to be able to supply the subject
product.
7. Submitting Rebuttal Comments.
[[Page 13263]]
Rebuttal Comments must meet the requirements outlined in 3 of these
procedures. General comments in support of or opposition to a Request
or a Response with an Offer do not meet the requirements of a Rebuttal
Comment. A Due Diligence Certification must accompany a Rebuttal
Comment.
(a) Rebuttal Comments. Any interested entity may submit a Rebuttal
Comment to a Response with an Offer submission. An interested entity
must submit its Rebuttal Comment not later than 4 U.S. business-days
after the deadline for Response with an Offer submission. If good cause
is shown, CITA may extend the time limit, but CITA will still meet the
statutory deadline for making a determination.
(b) Contents of a Rebuttal Comment. The Rebuttal Comment may respond
only to evidence or arguments raised in the Response with an Offer
submission and must identify the Response with an Offer submission,
evidence and/or arguments to which it is responding. The Rebuttal
Comment needs to reference the CITA File Number assigned to the
particular Commercial Availability Request being addressed.
8. Determination Process.
(a) Not later than 30 U.S. business days after official receipt of a
request (or not later than 44 U.S. business days where an extension is
provided), CITA will notify interested entities by email and interested
parties and the public by a posting on its website whether the subject
product is available in commercial quantities in a timely manner in the
CAFTA-DR countries and whether an interested entity has objected to the
request.
(b) CITA will notify the public of the determination by publication in
the Federal Register when the determination results in a change to the
Commercial Availability List in Annex 3.25 of the Agreement.
(c) Types of Determinations.
(1) Denial. A denial means that CITA has determined that the subject
product is available in commercial quantities in a timely manner in the
CAFTA-DR countries. If a request is denied, notice of the denial will
be posted on the CAFTA-DR Commercial Availability website at https://
web.ita.doc.gov/tacgi/CABroadcast.nsf/Document?Openform.
(2) Approval in Unrestricted Quantity. An approval in unrestricted
quantities means that CITA has determined that the subject product is
not available in commercial quantities in a timely manner in the CAFTA-
DR countries or that no interested entity has objected to the request.
(i) If a request is approved without restriction, a notice will be
published in the U.S. Federal Register not later than 30 U.S. business
days (or not more than 44 U.S. business days where an extension is
provided ) after the official receipt of a request, adding the subject
product to the Commercial Availability List in Annex 3.25 of the
Agreement.
(ii) The effective date of the determination is the date of
publication of the notice in the U.S. Federal Register.
(3) Approval in a Restricted Quantity.
(i) Approval in a Restricted Quantity. An Approval in a Restricted
Quantity means that CITA has determined to add the subject product to
the Commercial Availability List in Annex 3.25 of the Agreement with a
specified restricted quantity. CITA may approve the request in a
restricted quantity if CITA determines that a CAFTA-DR supplier(s) can
partially fulfill the request for the subject product. The restricted
quantity specifies the amount of the subject product that can be
provided by a CAFTA-DR supplier(s).
(A) If a request is approved in a restricted quantity, a notice
will be published in the Federal Register not later than 30 U.S.
business days (or not more the 44 U.S. business days where an extension
is provided ) after official receipt of the request, adding the subject
product to the Commercial Availability List in Annex 3.25 of the
Agreement with a specified restricted quantity. The restricted quantity
specifies the amount of the subject product that can be provided by a
CAFTA-DR supplier(s).
(B) The effective date of the determination will be the date of
publication in the U.S. Federal Register.
(ii) Elimination of a restricted quantity. Not later than six
months after adding a product to the Commercial Availability List in
Annex 3.25 of the Agreement in a restricted quantity, CITA may
eliminate the restriction if it determines that the subject product is
not available in commercial quantities in a timely manner in the CAFTA-
DR countries.
(A) The determination that the subject product is not available in
commercial quantities in a timely manner will be based upon whether the
restricted quantity has been provided by a CAFTA-DR supplier(s). CITA
will solicit comments and information from the CAFTA-DR supplier(s) and
the requester.
(B) If the CAFTA-DR supplier(s) are still capable of providing the
restricted quantity, the restriction will remain.
(C) If the CAFTA-DR supplier(s) are unable to provide the
restricted quantity, CITA will eliminate the restricted quantity. CITA
will publish a notice in the U.S. Federal Register, and post on the
website, that the restricted quantity is eliminated and the subject
product is added to the Commercial Availability List in Annex 3.25 in
an unrestricted quantity. The effective date of the determination will
be the date of publication in the U.S. Federal Register.
(4) Insufficient Information to Determine.CITA will extend its time
period for consideration of the Commercial Availability Request by an
additional 14 U.S. business days in the event that CITA determines, not
later than 30 U.S. business days after official receipt of a Commercial
Availability Request, that it has insufficient information to make a
determination regarding the ability of a CAFTA-DR supplier to supply
the subject products of the Commercial Availability Request based on
the submitted information. CITA will normally determine that it does
not have sufficient information to make a determination on a Commercial
Availability Request when CITA finds there is inconsistency in material
information contained in the Commercial Availability Request, one or
more Offers to Supply the subject product, and/or the Rebuttal
Comments. CITA will notify interested parties via email that it has
extended the time period for CITA's consideration by 14 U.S. business-
days. CITA also will announce the extension on the website.
(i) Process during Extension Period. During the extended time
period, CITA will request that interested entities provide additional
evidence to substantiate the information provided, and may initiate a
meeting with interested entities. Should CITA elect to conduct a
meeting, it will comply with
[[Page 13264]]
requirements to conduct proceedings in an open manner. Such evidence
may include inter alia product samples, lab tests, detailed
descriptions of product facilities, and comparisons of product
performance in the intended end-use of the subject product. Any
samples, if requested, of fibers, yarns, or fabrics, that are provided
to CITA will be made available for public inspection at the Office of
Textiles and Apparel, Room 3110, U.S. Department of Commerce, 14th St.
and Constitution Ave., N.W., Washington, DC 20230. All written
submissions must follow instructions described in section 3 of these
procedures. Samples should be identified with a cover sheet that
describes the specifications of the sample and be identical to the
specifications of the request.
(ii) CITA also will consider evidence in support of claims that
CAFTA-DR supplier(s) can supply a substantially similar product to that
specified in the request.
(iii) CITA will make a determination, not later than 44 U.S.
business days after the official receipt of a Commercial Availability
Request whether to Approve, Approve with Restriction, or Deny the
Commercial Availability Request and will follow the notification
process accordingly.
(5) Deemed Approval. In the event that CITA does not make a
determination in response to a Commercial Availability Request to add a
product to Annex 3.25 of the Agreement within the statutory deadlines
provided, not later than 45 U.S. business-days after the official
receipt of the commercial availability request or not later than 60
U.S. business-days after the official receipt of the Commercial
Availability Request that was determined to lack sufficient information
pursuant to subsection (c)(4), the requested subject product shall be
added to the Commercial Availability List in Annex 3.25 , in an
unrestricted quantity, in accordance with the requirements of section
203(o)(4)(D) of the CAFTA-DR Implementation Act. CITA will notify the
public of the Deemed Approval by publication in the U.S. Federal
Register and posting on OTEXA's website.
9. Six Month Procedures:
(a) Request to Remove or Restrict. No earlier than six months after a
product has been added to the Commercial Availability List in Annex
3.25 in an unrestricted quantity pursuant to sections 203(o)(2) and (4)
of the CAFTA-DR Implementation Act, an interested entity may submit a
request to CITA requesting that a product be either removed or that a
quantity restriction be introduced.
(b) Content of a Request to Remove or Restrict. The Request to Remove
or Restrict must provide the substantive information set forth in
subsection 6(b) (Contents of a Response with an Offer) of these
procedures.
(c) Procedures.
(1) In considering whether to accept a Request to Remove or Restrict,
CITA will follow procedures set forth in section 5 (Consideration and
Acceptance of a Request) of these procedures.
(2) If CITA determines to accept the Request to Remove or Restrict,
CITA and any responding interested entity shall follow applicable
procedures and contents set forth in subsections 6(a) (Response
Submission) and section 7 (Submitting Rebuttal Evidence) of these
procedures.
(3) As set forth in subsections 8(a) and (b) (Determination Process) of
these procedures, CITA will determine whether the subject product of
the Request to Remove or Restrict is available in commercial quantities
in a timely manner in the DR-CAFTA countries not later than 30 U.S.
business days after the official receipt of the request.
(i) If CITA determines that the product is available in commercial
quantities in a timely manner in the DR-CAFTA countries, e.g., that a
CAFTA-DR supplier is capable to supply the entire subject product
requested originally, then that product will be removed from the
Commercial Availability List in Annex 3.25 of the Agreement.
(ii) If CITA determines that the product is available in restricted
quantities in a timely manner in the CAFTA-DR countries, e.g., that a
CAFTA-DR supplier is capable to supply part of the subject product
requested originally then a restricted quantity will be introduced for
that product.
(iii) If the Commercial Availability List changes as a result of
CITA's determination for the Request to Remove or Restrict, CITA will
notify interested parties by email of its determination and will
publish a notice of its determination for the request to remove or
restrict in the U.S. Federal Register.
(A) For removal, the notice will state that textile and apparel
articles containing the subject product are not to be treated as
originating in a CAFTA-DR country if the subject product is obtained
from non- CAFTA-DR sources, effective for goods entered into the United
States on or after six months (i.e., 180 calendar days) after the date
of publication of the notice.
(B) For restriction, the notice will specify the restricted
quantity for the subject product that is to be effective on or after
six months (i.e., 180 calendar days) after the publication date of the
notice.
R. Matthew Priest,
Chairman, Committee for the Implementation of Textile Agreements.
[FR Doc. E7-5102 Filed 3-20-07; 8:45 am]
BILLING CODE 3510-DS-S