Foreign Supplier Verification Programs for Importers of Food for Humans and Animals; Extension of Comment Periods, 69602-69603 [2013-27645]
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69602
Federal Register / Vol. 78, No. 224 / Wednesday, November 20, 2013 / Proposed Rules
Piaggio Aero Industries S.p.A. Mandatory
Service Bulletin No.: 80–0381, Rev. 0, dated
May 2, 2013.
(2) If the clearance is less than 5 mm on
HS LH or RH side during the measurement
as required by paragraph (f)(1) of this AD,
before further flight, rework the affected
elevator to restore the required minimum
clearance between the horn of the elevator
and the end rib of the horizontal stabilizer
following Part B of the Accomplishment
Instructions section of Piaggio Aero
Industries S.p.A. Mandatory Service Bulletin
No.: 80–0381, Rev. 0, dated May 2, 2013.
(3) Within 30 days after accomplishment of
the measurement as required by paragraph
(f)(1) of this AD, report the results to Piaggio
Aero Industries S.p.A. following Part C of the
Accomplishment Instructions section of
Piaggio Aero Industries S.p.A. Mandatory
Service Bulletin No.: 80–0381, Rev. 0, dated
May 2, 2013.
pmangrum on DSK3VPTVN1PROD with PROPOSALS-1
(g) Other FAA AD Provisions
The following provisions also apply to this
AD:
(1) Alternative Methods of Compliance
(AMOCs): The Manager, Standards Office,
FAA, has the authority to approve AMOCs
for this AD, if requested using the procedures
found in 14 CFR 39.19. Send information to
ATTN: Mike Kiesov, Aerospace Engineer,
FAA, Small Airplane Directorate, 901 Locust,
Room 301, Kansas City, Missouri 64106;
telephone: (816) 329–4144; fax: (816) 329–
4090; email: mike.kiesov@faa.gov. Before
using any approved AMOC on any airplane
to which the AMOC applies, notify your
appropriate principal inspector (PI) in the
FAA Flight Standards District Office (FSDO),
or lacking a PI, your local FSDO.
(2) Airworthy Product: For any requirement
in this AD to obtain corrective actions from
a manufacturer or other source, use these
actions if they are FAA-approved. Corrective
actions are considered FAA-approved if they
are approved by the State of Design Authority
(or their delegated agent). You are required
to assure the product is airworthy before it
is returned to service.
(3) Reporting Requirements: For any
reporting requirement in this AD, a federal
agency may not conduct or sponsor, and a
person is not required to respond to, nor
shall a person be subject to a penalty for
failure to comply with a collection of
information subject to the requirements of
the Paperwork Reduction Act unless that
collection of information displays a current
valid OMB Control Number. The OMB
Control Number for this information
collection is 2120–0056. Public reporting for
this collection of information is estimated to
be approximately 5 minutes per response,
including the time for reviewing instructions,
completing and reviewing the collection of
information. All responses to this collection
of information are mandatory. Comments
concerning the accuracy of this burden and
suggestions for reducing the burden should
be directed to the FAA at: 800 Independence
Ave. SW., Washington, DC 20591, Attn:
Information Collection Clearance Officer,
AES–200.
VerDate Mar<15>2010
13:59 Nov 19, 2013
Jkt 232001
(h) Related Information
Refer to MCAI European Aviation Safety
Agency (EASA) AD No. 2013–0239, dated
September 30, 2013, for related information.
You may examine the MCAI on the Internet
at https://www.regulations.gov by searching
for and locating it in Docket No. FAA–2013–
0964. For service information related to this
AD, contact Piaggio Aero Industries S.p.A—
Airworthiness Office, Via Luigi Cibrario, 4–
16154 Genova-Italy; phone: +39 010 6481353;
fax: +39 010 6481881; email: Internet: https://
www.piaggioaero.com/#/en/aftersales/
service-support. You may review this
referenced service information at the FAA,
Small Airplane Directorate, 901 Locust,
Kansas City, Missouri 64106. For information
on the availability of this material at the
FAA, call (816) 329–4148.
Issued in Kansas City, Missouri, on
November 5, 2013.
Earl Lawrence,
Manager, Small Airplane Directorate, Aircraft
Certification Service.
[FR Doc. 2013–27639 Filed 11–19–13; 8:45 am]
BILLING CODE 4910–13–P
information collection provisions
associated with the rule consistent with
the comment period for the proposed
rule.
For the proposed rule published
on July 29, 2013 (78 FR 45730), submit
either electronic or written comments
by January 27, 2014. Submit comments
on information collection issues under
the Paperwork Reduction Act of 1995
(the PRA) by January 27, 2014 (see the
‘‘Paperwork Reduction Act of 1995’’
section of this document).
ADDRESSES: You may submit comments,
identified by Docket No. FDA–2011–N–
0143 and/or Regulatory Information
Number (RIN) 0910–AG64, by any of the
following methods, except that
comments on information collection
issues under the PRA must be submitted
to the Office of Information and
Regulatory Affairs, Office of
Management and Budget (OMB) (see the
‘‘Paperwork Reduction Act of 1995’’
section of this document).
DATES:
Electronic Submissions
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
21 CFR Part 1
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
[Docket No. FDA–2011–N–0143]
Written Submissions
Food and Drug Administration
RIN 0910–AG64
Foreign Supplier Verification Programs
for Importers of Food for Humans and
Animals; Extension of Comment
Periods
AGENCY:
Food and Drug Administration,
HHS.
Proposed rule; extension of
comment period for the proposed rule
and for its information collection
provisions.
ACTION:
The Food and Drug
Administration (FDA or we) is
extending the comment period for the
proposed rule, and for the information
collection related to the proposed rule
entitled ‘‘Foreign Supplier Verification
Programs for Importers of Food for
Humans and Animals’’ that appeared in
the Federal Register of July 29, 2013.
We are taking this action in response to
requests for an extension to allow
interested persons an opportunity to
consider the interrelationship between
this proposed rule and the proposed
rule announced in October 2013 entitled
‘‘Current Good Manufacturing Practice
and Hazard Analysis and Risk-Based
Preventive Controls for Food for
Animals.’’ We also are taking this action
to keep the comment period for the
SUMMARY:
PO 00000
Frm 00009
Fmt 4702
Sfmt 4702
Submit written submissions in the
following ways:
• Mail/Hand delivery/Courier (for
paper or CD–ROM submissions):
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville,
MD 20852.
Instructions: All submissions received
must include the Agency name, Docket
No. FDA–2011–N–0143, and RIN 0910–
AG64 for this rulemaking. All comments
received may be posted without change
to https://www.regulations.gov, including
any personal information provided. For
additional information on submitting
comments, see the ‘‘Request for
Comments’’ heading of the
SUPPLEMENTARY INFORMATION section of
this document.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
With regard to the proposed rule:
Brian Pendleton, Office of Policy, Food
and Drug Administration, 10903 New
E:\FR\FM\20NOP1.SGM
20NOP1
Federal Register / Vol. 78, No. 224 / Wednesday, November 20, 2013 / Proposed Rules
Hampshire Ave., Silver Spring, MD
20993–0002, 301–796–4614.
With regard to the information
collection: Domini Bean, Office of
Information Management, Food and
Drug Administration, 1350 Piccard Dr.,
PI50–400T, Rockville, MD 20850,
Domini.Bean@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
pmangrum on DSK3VPTVN1PROD with PROPOSALS-1
I. Background
In the Federal Register of July 29,
2013 (78 FR 45730), we published a
proposed rule entitled ‘‘Foreign
Supplier Verification Programs for
Importers of Food for Humans and
Animals’’ with a 120-day comment
period on the provisions of the
proposed rule and on the information
collection provisions that are subject to
review by OMB under the PRA (44
U.S.C. 3501–3520).
FDA has received requests for an
extension of the comment period on the
proposed rule to allow interested
persons an opportunity to consider the
interrelationship between this proposed
rule and the proposed rule entitled
‘‘Current Good Manufacturing Practice
and Hazard Analysis and Risk-Based
Preventive Controls for Food for
Animals’’ (78 FR 64736, October 29,
2013). FDA has considered the requests
and is granting a 60-day extension of the
comment period for the ‘‘Foreign
Supplier Verification Programs for
Importers of Food for Humans and
Animals’’ proposed rule to allow
interested persons an opportunity to
consider the interrelationships between
the proposed rules. We also are
extending the comment period for the
information collection provisions for 60
days to make the comment period for
the information collection provisions
the same as the comment period for the
provisions of the proposed rule. To
clarify, FDA is requesting comment on
all issues raised by the proposed rule.
II. Paperwork Reduction Act of 1995
Interested persons may either submit
electronic comments regarding the
information collection to oira_
submission@omb.eop.gov or fax written
comments to the Office of Information
and Regulatory Affairs, OMB, Attn: FDA
Desk Officer, FAX: 202–395–7285. All
comments should be identified with the
title ‘‘Foreign Supplier Verification
Programs for Importers of Food for
Humans and Animals.’’
III. Request for Comments
Interested persons may submit either
electronic comments regarding the
proposed rule to https://
www.regulations.gov or written
comments to the Division of Dockets
VerDate Mar<15>2010
13:59 Nov 19, 2013
Jkt 232001
Management (see ADDRESSES). It is only
necessary to send one set of comments.
Identify comments with the docket
number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday, and
will be posted to the docket at https://
www.regulations.gov.
Dated: November 13, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–27645 Filed 11–19–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
69603
by January 27, 2014. Submit comments
on information collection issues under
the Paperwork Reduction Act of 1995
(the PRA) by January 27, 2014 (see the
‘‘Paperwork Reduction Act of 1995’’
section of this document).
ADDRESSES: You may submit comments,
identified by Docket No. FDA–2011–N–
0146 and/or Regulatory Information
Number (RIN) 0910–AG66, by any of the
following methods, except that
comments on information collection
issues under the PRA must be submitted
to the Office of Information and
Regulatory Affairs, Office of
Management and Budget (OMB) (see the
‘‘Paperwork Reduction Act of 1995’’
section of this document).
Electronic Submissions
[Docket No. FDA–2011–N–0146]
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
RIN 0910–AG66
Written Submissions
Accreditation of Third-Party Auditors/
Certification Bodies To Conduct Food
Safety Audits and To Issue
Certifications; Extension of Comment
Periods
Submit written submissions in the
following ways:
• Mail/Hand delivery/Courier (for
paper or CD–ROM submissions):
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
Instructions: All submissions received
must include the Agency name, Docket
No. FDA–2011–N–0146, and RIN 0910–
AG66 for this rulemaking. All comments
received may be posted without change
to https://www.regulations.gov, including
any personal information provided. For
additional information on submitting
comments, see the ‘‘Request for
Comments’’ heading of the
SUPPLEMENTARY INFORMATION section of
this document.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
With regard to the proposed rule:
Charlotte Christin, Center for Food
Safety and Applied Nutrition, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 32, Rm. 4234,
Silver Spring, MD 20993–0002, 240–
402–3708.
With regard to the information
collection: Domini Bean, Office of
Information Management, Food and
Food and Drug Administration
21 CFR Parts 1 and 16
AGENCY:
Food and Drug Administration,
HHS.
Proposed rule; extension of
comment period for the proposed rule
and for its information collection
provisions.
ACTION:
The Food and Drug
Administration (FDA or we) is
extending the comment period for the
proposed rule, and for the information
collection related to the proposed rule
entitled ‘‘Accreditation of Third-Party
Auditors/Certification Bodies to
Conduct Food Safety Audits and to
Issue Certifications’’ that appeared in
the Federal Register of July 29, 2013.
We are taking this action in response to
requests for an extension to allow
interested persons an opportunity to
consider the interrelationship between
this proposed rule and the proposed
rule announced in October 2013 entitled
‘‘Current Good Manufacturing Practice
and Hazard Analysis and Risk-Based
Preventive Controls for Food for
Animals.’’ We also are taking this action
to keep the comment period for the
information collection provisions
associated with the rule consistent with
the comment period for the proposed
rule.
SUMMARY:
For the proposed rule published
on July 29, 2013 (78 FR 45782), submit
either electronic or written comments
DATES:
PO 00000
Frm 00010
Fmt 4702
Sfmt 4702
E:\FR\FM\20NOP1.SGM
20NOP1
]]>Agencies
[Federal Register Volume 78, Number 224 (Wednesday, November 20, 2013)]
[Proposed Rules]
[Pages 69602-69603]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-27645]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 1
[Docket No. FDA-2011-N-0143]
RIN 0910-AG64
Foreign Supplier Verification Programs for Importers of Food for
Humans and Animals; Extension of Comment Periods
AGENCY: Food and Drug Administration, HHS.
ACTION: Proposed rule; extension of comment period for the proposed
rule and for its information collection provisions.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is extending the
comment period for the proposed rule, and for the information
collection related to the proposed rule entitled ``Foreign Supplier
Verification Programs for Importers of Food for Humans and Animals''
that appeared in the Federal Register of July 29, 2013. We are taking
this action in response to requests for an extension to allow
interested persons an opportunity to consider the interrelationship
between this proposed rule and the proposed rule announced in October
2013 entitled ``Current Good Manufacturing Practice and Hazard Analysis
and Risk-Based Preventive Controls for Food for Animals.'' We also are
taking this action to keep the comment period for the information
collection provisions associated with the rule consistent with the
comment period for the proposed rule.
DATES: For the proposed rule published on July 29, 2013 (78 FR 45730),
submit either electronic or written comments by January 27, 2014.
Submit comments on information collection issues under the Paperwork
Reduction Act of 1995 (the PRA) by January 27, 2014 (see the
``Paperwork Reduction Act of 1995'' section of this document).
ADDRESSES: You may submit comments, identified by Docket No. FDA-2011-
N-0143 and/or Regulatory Information Number (RIN) 0910-AG64, by any of
the following methods, except that comments on information collection
issues under the PRA must be submitted to the Office of Information and
Regulatory Affairs, Office of Management and Budget (OMB) (see the
``Paperwork Reduction Act of 1995'' section of this document).
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Written Submissions
Submit written submissions in the following ways:
Mail/Hand delivery/Courier (for paper or CD-ROM
submissions): Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
Instructions: All submissions received must include the Agency
name, Docket No. FDA-2011-N-0143, and RIN 0910-AG64 for this
rulemaking. All comments received may be posted without change to
https://www.regulations.gov, including any personal information
provided. For additional information on submitting comments, see the
``Request for Comments'' heading of the SUPPLEMENTARY INFORMATION
section of this document.
Docket: For access to the docket to read background documents or
comments received, go to https://www.regulations.gov and insert the
docket number, found in brackets in the heading of this document, into
the ``Search'' box and follow the prompts and/or go to the Division of
Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
With regard to the proposed rule: Brian Pendleton, Office of
Policy, Food and Drug Administration, 10903 New
[[Page 69603]]
Hampshire Ave., Silver Spring, MD 20993-0002, 301-796-4614.
With regard to the information collection: Domini Bean, Office of
Information Management, Food and Drug Administration, 1350 Piccard Dr.,
PI50-400T, Rockville, MD 20850, Domini.Bean@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of July 29, 2013 (78 FR 45730), we
published a proposed rule entitled ``Foreign Supplier Verification
Programs for Importers of Food for Humans and Animals'' with a 120-day
comment period on the provisions of the proposed rule and on the
information collection provisions that are subject to review by OMB
under the PRA (44 U.S.C. 3501-3520).
FDA has received requests for an extension of the comment period on
the proposed rule to allow interested persons an opportunity to
consider the interrelationship between this proposed rule and the
proposed rule entitled ``Current Good Manufacturing Practice and Hazard
Analysis and Risk-Based Preventive Controls for Food for Animals'' (78
FR 64736, October 29, 2013). FDA has considered the requests and is
granting a 60-day extension of the comment period for the ``Foreign
Supplier Verification Programs for Importers of Food for Humans and
Animals'' proposed rule to allow interested persons an opportunity to
consider the interrelationships between the proposed rules. We also are
extending the comment period for the information collection provisions
for 60 days to make the comment period for the information collection
provisions the same as the comment period for the provisions of the
proposed rule. To clarify, FDA is requesting comment on all issues
raised by the proposed rule.
II. Paperwork Reduction Act of 1995
Interested persons may either submit electronic comments regarding
the information collection to oira_submission@omb.eop.gov or fax
written comments to the Office of Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX: 202-395-7285. All comments should be
identified with the title ``Foreign Supplier Verification Programs for
Importers of Food for Humans and Animals.''
III. Request for Comments
Interested persons may submit either electronic comments regarding
the proposed rule to https://www.regulations.gov or written comments to
the Division of Dockets Management (see ADDRESSES). It is only
necessary to send one set of comments. Identify comments with the
docket number found in brackets in the heading of this document.
Received comments may be seen in the Division of Dockets Management
between 9 a.m. and 4 p.m., Monday through Friday, and will be posted to
the docket at https://www.regulations.gov.
Dated: November 13, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-27645 Filed 11-19-13; 8:45 am]
BILLING CODE 4160-01-P
