Foreign-Trade Zone 61-San Juan, PR; Notification of Proposed Production Activity; Pfizer Pharmaceuticals LLC (Subzone 61A); (Ibuprofen Pharmaceutical Products); Guayama, PR, 36997-36998 [2012-15093]
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Federal Register / Vol. 77, No. 119 / Wednesday, June 20, 2012 / Notices
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MPCo. SMEPA determined that partial
ownership in the Project would help
minimize the unavoidable rate increase.
Based on these evaluations, SMEPA
determined that a 17.5% undivided
ownership interest in the Project would
be the best overall option and has
formally requested financial assistance
from RUS to finance this action.
SMEPA’s partial ownership would
include the IGCC facility, the CO2
pipeline, the reclaimed water supply
line, the surface lignite mine, and
electrical transmission facilities.
RUS Action
RUS conducts the rural electrification
loan program, which provides financing
through direct loans and loan
guarantees for the construction and
operation of generation facilities and
electric transmission and distribution
lines and systems to improve electric
service for rural Americans. RUS bases
its decisions on financial, engineering,
and environmental considerations. RUS
assessed whether SMEPA would have
sufficient control and responsibility to
alter the development of the Project in
order to determine if the project is
subject to NEPA, in accordance with 7
CFR 1794.20. Through discussions with
SMEPA, and review of loan and
contractual documentation, RUS
established that the project will be
completed regardless of RUS-funded
SMEPA participation. RUS further
established that the Joint Ownership
and Operating Agreement (JOOA), to be
executed with MPCo, will provide
SMEPA with only a limited ability to
influence the Project.2 However, due to
the Project’s significant public interest
and potential federal expenditure, RUS
decided to consider the Project a federal
action subject to NEPA and an
undertaking as defined by Section 106
of the NHPA.
RUS reviewed transmission system
impact studies and additional
engineering studies provided by
SMEPA, and the Final EIS (FEIS) and
the associated MAP prepared by the
DOE in cooperation with the USACE.
RUS determined that SMEPA’s
participation would not require any
additional infrastructure, and therefore
would not cause any environmental
impacts beyond what was identified and
discussed in the FEIS. RUS reviewed
and determined that the FEIS and MAP
2 Through the JOOA, SMEPA would only be
granted audit rights and authority for on-site
representation during Project construction and
operation. Should a Project Management Committee
(PMC) be formed, SMEPA’s representation would
be proportional to their percentage of ownership,
and therefore limited to 17.5% influence over
construction and management decisions.
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36997
adequately assessed the potential
impacts of the Project, and intends to
adopt the EIS in accordance with 40
CFR 1506.3 and 7 CFR 1794.72. RUS/
SMEPA participation will not cause any
additional impacts on historic
properties. RUS has therefore
determined that the Project qualifies as
an undertaking with no potential to
effect historic properties in accordance
with 36 CFR 800.3(a)(1).
This notice documents the Agency’s
intent to adopt the DOE/USACE FEIS,
and fulfills the agency’s responsibilities
for public involvement, in accordance
with 36 CFR 800.2(d)(2).
Secretary at the address below. The
closing period for their receipt is July
30, 2012.
A copy of the notification will be
available for public inspection at the
Office of the Executive Secretary,
Foreign-Trade Zones Board, Room 2111,
U.S. Department of Commerce, 1401
Constitution Avenue NW., Washington,
DC 20230–0002, and in the ‘‘Reading
Room’’ section of the Board’s Web site,
which is accessible via www.trade.gov/
ftz.
For further information, contact Diane
Finver at Diane.Finver@trade.gov or
(202) 482–1367.
Nivin Elgohary,
Assistant Administrator, Electric Programs,
Rural Utilities Service.
Elizabeth Whiteman,
Acting Executive Secretary.
[FR Doc. 2012–15035 Filed 6–19–12; 8:45 am]
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[FR Doc. 2012–15088 Filed 6–19–12; 8:45 am]
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DEPARTMENT OF COMMERCE
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–44–2012]
[B–45–2012]
Foreign-Trade Zone 7—Mayaguez, PR;
Notification of Proposed Production
Activity; Baxter Healthcare of Puerto
Rico; (Pharmaceutical and Nutritional
Intravenous Bags and Administration
Sets); Aibonito and Jayuya, PR
The Puerto Rico Industrial
Development Company, grantee of FTZ
7, submitted a notification of proposed
production activity on behalf of Baxter
Healthcare of Puerto Rico (Baxter), at
two sites within FTZ 7, located in
Aibonito and Jayuya, Puerto Rico. The
facilities are used for the manufacture of
pharmaceutical and nutritional
intravenous (I.V.) bags, I.V.
administration sets and their
components.
Production under FTZ procedures
could exempt Baxter from customs duty
payments on the foreign status
components used in export production.
On its domestic sales, Baxter would be
able to choose the duty rates during
customs entry procedures that apply to
the filled I.V. products and
administration sets) (duty-free) for the
foreign status inputs noted below.
Customs duties also could possibly be
deferred or reduced on foreign status
production equipment.
Components and materials sourced
from abroad include: Foil pouches, ABS
resin, L-tryptophan, glutamic acid, NAcetyl-L-Tyrosine and L-Lysine-Acetate
(duty rate range: 3%–6.5%).
Public comment is invited from
interested parties. Submissions shall be
addressed to the Board’s Executive
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Foreign-Trade Zones Board
Foreign-Trade Zone 61—San Juan, PR;
Notification of Proposed Production
Activity; Pfizer Pharmaceuticals LLC
(Subzone 61A); (Ibuprofen
Pharmaceutical Products); Guayama,
PR
The Puerto Rico Trade and Export
Company, grantee of FTZ 61, submitted
a notification of proposed production
activity on behalf of Pfizer
Pharmaceuticals LLC (Pfizer) (Subzone
61A) for its manufacturing facility
located in Guayama, Puerto Rico. The
notification conforming to the
requirements of the regulations of the
Board (15 CFR 400.22) was received on
June 13, 2012.
Subzone 61A was originally approved
by the Board in 1992 at the former
Searle plant located at Munoz Marin
Avenue and Road 189 in Caguas, Puerto
Rico, for the production and
distribution of various pharmaceutical
products under zone procedures (Board
Order 617, 12/11/1992, 57 FR 61046,
12/23/1992). On June 8, 2012, a minor
boundary modification under 15 CFR
400.38 of the Board’s regulations was
approved to relocate the subzone from
Pfizer’s Caguas plant to its facility
located at PR 2, Km 141.3 in Guayama,
Puerto Rico (S–69–2012).
Pfizer is now requesting to produce
ibuprofen pharmaceutical products in
bulk mixture or dosage form under FTZ
procedures at the Guayama site.
Production under FTZ procedures could
exempt Pfizer from customs duty
payments on the foreign status
components used in export production.
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36998
Federal Register / Vol. 77, No. 119 / Wednesday, June 20, 2012 / Notices
On its domestic sales, Pfizer would be
able to choose the duty rate during
customs entry procedures that applies to
the ibuprofen pharmaceutical products
(duty-free) for foreign-status ibuprofen
active ingredient (duty rate, 6.5%).
Customs duties also could possibly be
deferred or reduced on foreign-status
production equipment.
Public comment is invited from
interested parties. Submissions shall be
addressed to the Board’s Executive
Secretary at the address below. The
closing period for their receipt is July
30, 2012.
A copy of the notification will be
available for public inspection at the
Office of the Executive Secretary,
Foreign-Trade Zones Board, Room 2111,
U.S. Department of Commerce, 1401
Constitution Avenue NW., Washington,
DC 20230–0002, and in the ‘‘Reading
Room’’ section of the Board’s Web site,
which is accessible via www.trade.gov/
ftz.
For further information, contact Diane
Finver at Diane.Finver@trade.gov or
(202) 482–1367.
Elizabeth Whiteman,
Acting Executive Secretary.
[FR Doc. 2012–15093 Filed 6–19–12; 8:45 am]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
Proposed Information Collection;
Comment Request; Mandatory Shrimp
Vessel and Gear Characterization
Survey
National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice.
AGENCY:
The Department of
Commerce, as part of its continuing
effort to reduce paperwork and
respondent burden, invites the general
public and other Federal agencies to
take this opportunity to comment on
proposed and/or continuing information
collections, as required by the
Paperwork Reduction Act of 1995.
DATES: Written comments must be
submitted on or before August 20, 2012.
ADDRESSES: Direct all written comments
to Jennifer Jessup, Departmental
Paperwork Clearance Officer,
Department of Commerce, Room 6616,
14th and Constitution Avenue NW.,
Washington, DC 20230 (or via the
Internet at JJessup@doc.gov).
FOR FURTHER INFORMATION CONTACT:
Requests for additional information or
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SUMMARY:
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copies of the information collection
instrument and instructions should be
directed to Anik Clemens, (727) 551–
5611 or Anik.Clemens@noaa.gov.
SUPPLEMENTARY INFORMATION:
I. Abstract
This request is for extension of a
current information collection.
The Magnuson-Stevens Fishery
Conservation and Management Act
(Magnuson-Stevens Act) authorizes the
Gulf of Mexico Fishery Management
Council (Council) to prepare and amend
fishery management plans for any
fishery in waters under its jurisdiction.
National Marine Fisheries Service
(NMFS) manages the shrimp fishery in
the waters of the Gulf of Mexico under
the Shrimp Fishery Management Plan
(FMP). The regulations for the Gulf
Shrimp Vessel and Gear
Characterization Form may be found at
50 CFR 622.5(a)(1)(iii)(C).
Owners or operators of vessels
applying for or renewing a commercial
vessel moratorium permit for Gulf
shrimp must complete an annual Gulf
Shrimp Vessel and Gear
Characterization Form. The form will be
provided by NMFS at the time of permit
application and renewal. Compliance
with this reporting requirement is
required for permit issuance and
renewal.
Through this form, NMFS is
collecting census-level information on
fishing vessel and gear characteristics in
the Gulf of Mexico Exclusive Economic
Zone (EEZ) shrimp fishery to conduct
analyses that will improve fishery
management decision-making in this
fishery; ensure that national goals,
objectives, and requirements of the
Magnuson-Stevens Act, National
Environmental Policy Act (NEPA),
Regulatory Flexibility Act (RFA),
Endangered Species Act (ESA), and
Executive Order (E.O.) 12866 are met;
and quantify achievement of the
performance measures in the NMFS’
Operating Plans. This information is
vital in assessing the economic, social,
and environmental effects of fishery
management decisions and regulations
on individual shrimp fishing
enterprises, fishing communities, and
the nation as a whole.
The burden estimates for this
information collection have changed
due to adjustments. Currently, there are
approximately 1,563 permitted vessels
in the Gulf shrimp fishery—fewer
vessels than in the previous renewal.
II. Method of Collection
Respondents are mailed hard copies
of the form. The forms must be
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completed and mailed back to NMFS
before their permits expire.
III. Data
OMB Control Number: 0648–0542.
Form Number: None.
Type of Review: Regular submission
(extension of a current information
collection).
Affected Public: Business or other forprofit organizations.
Estimated Number of Respondents:
1,563.
Estimated Time per Response:
Reports, 20 minutes.
Estimated Total Annual Burden
Hours: 521.
Estimated Total Annual Cost to
Public: $0 in recordkeeping/reporting
costs.
IV. Request for Comments
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden
(including hours and cost) of the
proposed collection of information;
(c) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (d) ways to minimize
the burden of the collection of
information on respondents, including
through the use of automated collection
techniques or other forms of information
technology.
Comments submitted in response to
this notice will be summarized and/or
included in the request for OMB
approval of this information collection;
they also will become a matter of public
record.
Dated: June 14, 2012.
Gwellnar Banks,
Management Analyst, Office of the Chief
Information Officer.
[FR Doc. 2012–14987 Filed 6–19–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
Notice of Availability of a Draft
Programmatic Environmental
Assessment for Office of Coast Survey
Hydrographic Survey Projects
Office of Coast Survey (OCS),
National Ocean Service (NOS), National
Oceanic and Atmospheric
Administration (NOAA), Department of
Commerce.
AGENCY:
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Agencies
[Federal Register Volume 77, Number 119 (Wednesday, June 20, 2012)]
[Notices]
[Pages 36997-36998]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-15093]
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DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B-44-2012]
Foreign-Trade Zone 61--San Juan, PR; Notification of Proposed
Production Activity; Pfizer Pharmaceuticals LLC (Subzone 61A);
(Ibuprofen Pharmaceutical Products); Guayama, PR
The Puerto Rico Trade and Export Company, grantee of FTZ 61,
submitted a notification of proposed production activity on behalf of
Pfizer Pharmaceuticals LLC (Pfizer) (Subzone 61A) for its manufacturing
facility located in Guayama, Puerto Rico. The notification conforming
to the requirements of the regulations of the Board (15 CFR 400.22) was
received on June 13, 2012.
Subzone 61A was originally approved by the Board in 1992 at the
former Searle plant located at Munoz Marin Avenue and Road 189 in
Caguas, Puerto Rico, for the production and distribution of various
pharmaceutical products under zone procedures (Board Order 617, 12/11/
1992, 57 FR 61046, 12/23/1992). On June 8, 2012, a minor boundary
modification under 15 CFR 400.38 of the Board's regulations was
approved to relocate the subzone from Pfizer's Caguas plant to its
facility located at PR 2, Km 141.3 in Guayama, Puerto Rico (S-69-2012).
Pfizer is now requesting to produce ibuprofen pharmaceutical
products in bulk mixture or dosage form under FTZ procedures at the
Guayama site. Production under FTZ procedures could exempt Pfizer from
customs duty payments on the foreign status components used in export
production.
[[Page 36998]]
On its domestic sales, Pfizer would be able to choose the duty rate
during customs entry procedures that applies to the ibuprofen
pharmaceutical products (duty-free) for foreign-status ibuprofen active
ingredient (duty rate, 6.5%). Customs duties also could possibly be
deferred or reduced on foreign-status production equipment.
Public comment is invited from interested parties. Submissions
shall be addressed to the Board's Executive Secretary at the address
below. The closing period for their receipt is July 30, 2012.
A copy of the notification will be available for public inspection
at the Office of the Executive Secretary, Foreign-Trade Zones Board,
Room 2111, U.S. Department of Commerce, 1401 Constitution Avenue NW.,
Washington, DC 20230-0002, and in the ``Reading Room'' section of the
Board's Web site, which is accessible via www.trade.gov/ftz.
For further information, contact Diane Finver at
Diane.Finver@trade.gov or (202) 482-1367.
Elizabeth Whiteman,
Acting Executive Secretary.
[FR Doc. 2012-15093 Filed 6-19-12; 8:45 am]
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