Foreign-Trade Zone Subzone 22- Chicago, IL, Temporary/Interim Manufacturing Authority, Baxter Healthcare Corporation (Pharmaceutical and Biological Product Manufacturing), Notice of Approval, 9743-9744 [2011-3890]
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Federal Register / Vol. 76, No. 35 / Tuesday, February 22, 2011 / Notices
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Dated in Washington, DC, on February 15,
2011.
Peter Minarik,
Acting Chief, Regional Programs
Coordination Unit.
[FR Doc. 2011–3814 Filed 2–18–11; 8:45 am]
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Dated: February 4, 2011.
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Analysis.
[FR Doc. 2011–3652 Filed 2–18–11; 8:45 am]
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DEPARTMENT OF COMMERCE
Economics and Statistics
Administration
DEPARTMENT OF COMMERCE
Bureau of Economic Analysis Advisory
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Bureau of Economic Analysis,
Commerce.
ACTION: Notice of public meeting.
AGENCY:
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SUMMARY:
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Foreign-Trade Zones Board
[Order No. 1739]
Approval for Expanded Manufacturing
Authority, Foreign-Trade Subzone
116A, Motiva Enterprises, LLC (Oil
Refinery), Port Arthur, TX
Pursuant to its authority under the ForeignTrade Zones Act of June 18, 1934, as
amended (19 U.S.C. 81a–81u), the ForeignTrade Zones Board (the Board) adopts the
following Order:
Whereas, the Foreign-Trade Zone of
Southeast Texas, grantee of ForeignTrade Zone 116, has requested authority
on behalf of Motiva Enterprises, LLC
(Motiva), to expand the scope of
manufacturing activity conducted under
zone procedures within Subzone 116A
at the Motiva facilities in Port Arthur,
Texas, (FTZ Docket 43–2010, filed 7–1–
2010);
Whereas, notice inviting public
comment has been given in the Federal
Register (75 FR 39662–39663, 7–15–
2010) and the application has been
processed pursuant to the FTZ Act and
the Board’s regulations; and,
Whereas, the Board adopts the
findings and recommendations of the
examiner’s report, and finds that the
requirements of the FTZ Act and
Board’s regulations would be satisfied,
and that the proposal would be in the
public interest if subject to the
restrictions listed below;
Now, therefore, the Board hereby
orders:
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9743
The application to expand the scope
of manufacturing authority under zone
procedures within Subzone 116A, as
described in the application and
Federal Register notice, is approved,
subject to the FTZ Act and the Board’s
regulations, including Section 400.28,
and further subject to the following
restrictions:
1. Foreign status (19 CFR 146.41, 146.42)
products consumed as fuel for the refinery
shall be subject to the applicable duty rate.
2. Privileged foreign status (19 CFR 146.41)
shall be elected on all foreign merchandise
admitted to the subzone, except that nonprivileged foreign (NPF) status (19 CFR
146.42) may be elected on refinery inputs
covered under HTSUS Subheadings
#2709.00.10, #2709.00.20, #2710.11.25,
#2710.11.45, #2710.19.05, #2710.19.10,
#2710.19.45, #2710.91.00, #2710.99.05,
#2710.99.10, #2710.99.16, #2710.99.21 and
#2710.99.45 which are used in the
production of:
—petrochemical feedstocks and refinery byproducts (examiner’s report, Appendix
‘‘C’’);
—products for export;
—and, products eligible for entry under
HTSUS #9808.00.30 and #9808.00.40 (U.S.
Government purchases).
Signed at Washington, DC, this 4th day of
February 2011.
Ronald K. Lorentzen,
Deputy Assistant Secretary for Import
Administration, Alternate Chairman, ForeignTrade Zones Board.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2011–3894 Filed 2–18–11; 8:45 am]
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DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[T–1–2011]
Foreign-Trade Zone Subzone 22—
Chicago, IL, Temporary/Interim
Manufacturing Authority, Baxter
Healthcare Corporation
(Pharmaceutical and Biological
Product Manufacturing), Notice of
Approval
On January 18, 2011, the Executive
Secretary of the Foreign-Trade Zones
(FTZ) Board filed an application
submitted by the Illinois International
Port District, grantee of FTZ 22,
requesting temporary/interim
manufacturing (T/IM) authority, on
behalf of Baxter Healthcare Corporation
(Baxter) to manufacture pharmaceutical
and biological intravenous (I.V.)
products under FTZ procedures within
FTZ 22—Site 21, in Round Lake,
Illinois.
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Federal Register / Vol. 76, No. 35 / Tuesday, February 22, 2011 / Notices
The application was processed in
accordance with T/IM procedures, as
authorized by FTZ Board Orders 1347
(69 FR 52857, 8/30/04) and 1480 (71 FR
55422, 9/22/06). The Baxter facility and
activity in question had initially been
proposed to the FTZ Board for subzone
authority, including notice in the
Federal Register inviting public
comment (FTZ Doc. 60–2010, 75 FR
65448, 10/25/2010). To enable
expedited authority for Baxter in the
context of the FTZ Board’s recent
approval of the reorganization of FTZ 22
under the alternative site framework
(ASF) (Board Order 1738, 1/12/2011, 76
FR 4285, 1/25/2011), FTZ 22
subsequently requested to designate the
Baxter facility as a usage-driven site
(Site 21, A27f-2–2011, 1/14/2011), and
requested T/IM authority for Baxter’s
manufacturing of I.V. products. The
foreign-origin component approved for
this activity is laminated film (HTSUS
3920.10). The FTZ staff examiner
reviewed the application and
determined that it meets the criteria for
approval under T/IM procedures. As
noted above, public comment had been
sought on the specific proposed activity
through the Federal Register notice
published regarding the proposed
subzone authority (FTZ Doc. 60–2010).
Pursuant to the authority delegated to
the FTZ Board Executive Secretary in
the above-referenced Board Orders, the
application for T/IM authority is
approved, effective this date, until
February 11, 2013, subject to the FTZ
Act and the Board’s regulations,
including Section 400.28.
Dated: February 11, 2011.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2011–3890 Filed 2–18–11; 8:45 am]
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DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[Order No. 1741]
Reorganization of Foreign-Trade Zone
181 under Alternative Site Framework;
Akron/Canton, OH
Whereas, the Northeast Ohio Trade &
Economic Consortium, grantee of
Foreign-Trade Zone 181, submitted an
application to the Board (FTZ Docket
49–2010, filed 8/17/2010) for authority
to reorganize under the ASF with a
service area of Ashtabula, Trumbull,
Mahoning, Columbiana, Portage,
Summit, Stark, Medina, Wayne and
Richland Counties, Ohio, adjacent to the
Cleveland Customs and Border
Protection port of entry, FTZ 181’s
existing Sites 1, 3–6, and 8–27 would be
categorized as magnet sites, and the
grantee proposes an additional magnet
site (Site 29);
Whereas, notice inviting public
comment was given in the Federal
Register (75 FR 51753–51754, 8/23/
2010) and the application has been
processed pursuant to the FTZ Act and
the Board’s regulations; and,
Whereas, the Board adopts the
findings and recommendation of the
examiner’s report, and finds that the
requirements of the FTZ Act and
Board’s regulations are satisfied, and
that the proposal is in the public
interest;
Now, therefore, the Board hereby
orders:
The application to reorganize FTZ 181
under the alternative site framework is
approved, subject to the FTZ Act and
the Board’s regulations, including
Section 400.28, to the Board’s standard
2,000-acre activation limit for the
overall general-purpose zone project, to
a five-year ASF sunset provision for
magnet sites that would terminate
authority for Sites 3–5, 8, 10, 11, 14–21,
23, 25–27 and 29 if not activated by
February 29, 2016, and to a seven-year
ASF sunset provision for magnet sites
that would terminate authority for Sites
6, 9, 12, 13, 22 and 24 if not activated
by February 28, 2018.
Signed at Washington, DC, this 4th day of
February, 2011.
Ronald K. Lorentzen,
Deputy Assistant Secretary for Import
Administration, Alternate Chairman, ForeignTrade Zones Board.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2011–3895 Filed 2–18–11; 8:45 am]
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Pursuant to its authority under the ForeignTrade Zones Act of June 18, 1934, as
amended (19 U.S.C. 81a–81u), the ForeignTrade Zones Board (the Board) adopts the
following Order:
Whereas, the Board adopted the
alternative site framework (ASF) (74 FR
1170, 01/12/09; correction 74 FR 3987,
01/22/09; 75 FR 71069–71070, 11/22/
10) as an option for the establishment or
reorganization of general-purpose zones;
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DEPARTMENT OF COMMERCE
Bureau of Industry and Security
Regulations and Procedures Technical
Advisory Committee; Notice of
Partially Closed Meeting
The Regulations and Procedures
Technical Advisory Committee (RPTAC)
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will meet March 15, 2011, 9 a.m., Room
4830, in the Herbert C. Hoover Building,
14th Street between Constitution and
Pennsylvania Avenues, NW.,
Washington, DC. The Committee
advises the Office of the Assistant
Secretary for Export Administration on
implementation of the Export
Administration Regulations (EAR) and
provides for continuing review to
update the EAR as needed.
Agenda
Public Session
1. Opening remarks by the Chairman.
2. Opening remarks by Bureau of
Industry and Security.
3. Export Enforcement update.
4. Regulations update.
5. Working group reports.
6. Automated Export System (AES)
update.
7. Presentation of papers or comments
by the Public.
Closed Session
8. Discussion of matters determined to
be exempt from the provisions relating
to public meetings found in 5 U.S.C.
app. 2 §§ 10(a)(1) and 10(a)(3).
The open session will be accessible
via teleconference to 20 participants on
a first come, first serve basis. To join the
conference, submit inquiries to Ms.
Yvette Springer at
Yspringer@bis.doc.gov no later than
March 8, 2011.
A limited number of seats will be
available for the public session.
Reservations are not accepted. To the
extent that time permits, members of the
public may present oral statements to
the Committee. The public may submit
written statements at any time before or
after the meeting. However, to facilitate
the distribution of public presentation
materials to the Committee members,
the Committee suggests that presenters
forward the public presentation
materials prior to the meeting to Ms.
Springer via e-mail.
The Assistant Secretary for
Administration, with the concurrence of
the delegate of the General Counsel,
formally determined on February 9,
2011, pursuant to Section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. app. 2 §§ (10)(d)),
that the portion of the meeting dealing
with matters the disclosure of which
would be likely to frustrate significantly
implementation of an agency action as
described in 5 U.S.C. 552b(c)(9)(B) shall
be exempt from the provisions relating
to public meetings found in 5 U.S.C.
app. 2 §§ 10(a)(1) and 10(a)(3). The
remaining portions of the meeting will
be open to the public.
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Agencies
[Federal Register Volume 76, Number 35 (Tuesday, February 22, 2011)]
[Notices]
[Pages 9743-9744]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-3890]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[T-1-2011]
Foreign-Trade Zone Subzone 22-- Chicago, IL, Temporary/Interim
Manufacturing Authority, Baxter Healthcare Corporation (Pharmaceutical
and Biological Product Manufacturing), Notice of Approval
On January 18, 2011, the Executive Secretary of the Foreign-Trade
Zones (FTZ) Board filed an application submitted by the Illinois
International Port District, grantee of FTZ 22, requesting temporary/
interim manufacturing (T/IM) authority, on behalf of Baxter Healthcare
Corporation (Baxter) to manufacture pharmaceutical and biological
intravenous (I.V.) products under FTZ procedures within FTZ 22--Site
21, in Round Lake, Illinois.
[[Page 9744]]
The application was processed in accordance with T/IM procedures,
as authorized by FTZ Board Orders 1347 (69 FR 52857, 8/30/04) and 1480
(71 FR 55422, 9/22/06). The Baxter facility and activity in question
had initially been proposed to the FTZ Board for subzone authority,
including notice in the Federal Register inviting public comment (FTZ
Doc. 60-2010, 75 FR 65448, 10/25/2010). To enable expedited authority
for Baxter in the context of the FTZ Board's recent approval of the
reorganization of FTZ 22 under the alternative site framework (ASF)
(Board Order 1738, 1/12/2011, 76 FR 4285, 1/25/2011), FTZ 22
subsequently requested to designate the Baxter facility as a usage-
driven site (Site 21, A27f-2-2011, 1/14/2011), and requested T/IM
authority for Baxter's manufacturing of I.V. products. The foreign-
origin component approved for this activity is laminated film (HTSUS
3920.10). The FTZ staff examiner reviewed the application and
determined that it meets the criteria for approval under T/IM
procedures. As noted above, public comment had been sought on the
specific proposed activity through the Federal Register notice
published regarding the proposed subzone authority (FTZ Doc. 60-2010).
Pursuant to the authority delegated to the FTZ Board Executive
Secretary in the above-referenced Board Orders, the application for T/
IM authority is approved, effective this date, until February 11, 2013,
subject to the FTZ Act and the Board's regulations, including Section
400.28.
Dated: February 11, 2011.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2011-3890 Filed 2-18-11; 8:45 am]
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