Foreign-Trade Zone 153-San Diego, CA; Application for Manufacturing Authority; Abbott Cardiovascular Systems, Inc. (Cardiovascular Device Manufacturing); Riverside County, CA, 4283 [2011-1506]
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Federal Register / Vol. 76, No. 16 / Tuesday, January 25, 2011 / Notices
LIST OF PETITIONS RECEIVED BY EDA FOR CERTIFICATION OF ELIGIBILITY TO APPLY FOR TRADE ADJUSTMENT
ASSISTANCE 1/6/2011 THROUGH 1/19/2011—Continued
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Dated: January 19, 2011.
Miriam Kearse,
Eligibility Certifier.
[FR Doc. 2011–1450 Filed 1–24–11; 8:45 am]
BILLING CODE 3510–24–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[Docket 6–2011]
mstockstill on DSKH9S0YB1PROD with NOTICES
Foreign-Trade Zone 153—San Diego,
CA; Application for Manufacturing
Authority; Abbott Cardiovascular
Systems, Inc. (Cardiovascular Device
Manufacturing); Riverside County, CA
An application has been submitted to
the Foreign-Trade Zones Board (the
Board) by the City of San Diego, grantee
of FTZ 153, requesting manufacturing
authority on behalf of Abbott
Cardiovascular Systems, Inc. (Abbott),
located in Riverside County, California.
The application was submitted pursuant
to the provisions of the Foreign-Trade
VerDate Mar<15>2010
18:40 Jan 24, 2011
Jkt 223001
Rochester,
06–Jan–11 ............
Zones Act, as amended (19 U.S.C. 81a–
81u), and the regulations of the Board
(15 CFR part 400). It was formally filed
on January 18, 2011.
The Abbott facilities (3,500
employees, up to 9 million units per
year) are located within three sites of
FTZ 153: Site 11 (54.2 acres) is located
at 26531 Ynez Road, Temecula; Site 12
(8.3 acres) is located at 42301 Zevo
Drive, Temecula; and, Site 13 (4.4 acres)
is located at 30590 Cochise Circle,
Murrieta. The facilities are used for the
production of cardiovascular devices
including stents, catheters and
guidewires. Components and materials
sourced from abroad (representing 5%
of the value of the finished product)
include: resins, plastic tubing, stent
components, plastic packaging, plastic
clips, nickel tubing and tantalum tubing
(duty rate ranges from 2 to 6.5%). The
application also requests authority to
include a broad range of inputs and
finished cardiovascular devices that
Abbott may produce under FTZ
procedures in the future. New major
activity involving these inputs/products
would require review by the FTZ Board.
FTZ procedures could exempt Abbott
from customs duty payments on the
foreign components used in export
production. The company anticipates
that some 50 percent of the plants’
shipments will be exported. On its
domestic sales, Abbott would be able to
choose the duty rate during customs
entry procedures that applies to the
finished cardiovascular devices (duty
free) for the foreign inputs noted above.
FTZ designation would further allow
Abbott to realize logistical benefits
through the use of weekly customs entry
procedures. Customs duties also could
possibly be deferred or reduced on
foreign status production equipment.
PO 00000
Frm 00006
Fmt 4703
Sfmt 9990
The request indicates that the savings
from FTZ procedures would help
improve the facilities’ international
competitiveness.
In accordance with the Board’s
regulations, Diane Finver of the FTZ
Staff is designated examiner to evaluate
and analyze the facts and information
presented in the application and case
record and to report findings and
recommendations to the Board.
Public comment is invited from
interested parties. Submissions (original
and 3 copies) shall be addressed to the
Board’s Executive Secretary at the
address below. The closing period for
their receipt is March 28, 2011. Rebuttal
comments in response to material
submitted during the foregoing period
may be submitted during the subsequent
15-day period to April 11, 2011.
A copy of the application 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 https://
www.trade.gov/ftz.
For further information, contact Diane
Finver at Diane.Finver@trade.gov or
(202) 482–1367.
Dated: January 18, 2011.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2011–1506 Filed 1–24–11; 8:45 am]
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E:\FR\FM\25JAN1.SGM
25JAN1
Agencies
[Federal Register Volume 76, Number 16 (Tuesday, January 25, 2011)]
[Notices]
[Page 4283]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-1506]
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DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[Docket 6-2011]
Foreign-Trade Zone 153--San Diego, CA; Application for
Manufacturing Authority; Abbott Cardiovascular Systems, Inc.
(Cardiovascular Device Manufacturing); Riverside County, CA
An application has been submitted to the Foreign-Trade Zones Board
(the Board) by the City of San Diego, grantee of FTZ 153, requesting
manufacturing authority on behalf of Abbott Cardiovascular Systems,
Inc. (Abbott), located in Riverside County, California. The application
was submitted pursuant to the provisions of the Foreign-Trade Zones
Act, as amended (19 U.S.C. 81a-81u), and the regulations of the Board
(15 CFR part 400). It was formally filed on January 18, 2011.
The Abbott facilities (3,500 employees, up to 9 million units per
year) are located within three sites of FTZ 153: Site 11 (54.2 acres)
is located at 26531 Ynez Road, Temecula; Site 12 (8.3 acres) is located
at 42301 Zevo Drive, Temecula; and, Site 13 (4.4 acres) is located at
30590 Cochise Circle, Murrieta. The facilities are used for the
production of cardiovascular devices including stents, catheters and
guidewires. Components and materials sourced from abroad (representing
5% of the value of the finished product) include: resins, plastic
tubing, stent components, plastic packaging, plastic clips, nickel
tubing and tantalum tubing (duty rate ranges from 2 to 6.5%). The
application also requests authority to include a broad range of inputs
and finished cardiovascular devices that Abbott may produce under FTZ
procedures in the future. New major activity involving these inputs/
products would require review by the FTZ Board.
FTZ procedures could exempt Abbott from customs duty payments on
the foreign components used in export production. The company
anticipates that some 50 percent of the plants' shipments will be
exported. On its domestic sales, Abbott would be able to choose the
duty rate during customs entry procedures that applies to the finished
cardiovascular devices (duty free) for the foreign inputs noted above.
FTZ designation would further allow Abbott to realize logistical
benefits through the use of weekly customs entry procedures. Customs
duties also could possibly be deferred or reduced on foreign status
production equipment. The request indicates that the savings from FTZ
procedures would help improve the facilities' international
competitiveness.
In accordance with the Board's regulations, Diane Finver of the FTZ
Staff is designated examiner to evaluate and analyze the facts and
information presented in the application and case record and to report
findings and recommendations to the Board.
Public comment is invited from interested parties. Submissions
(original and 3 copies) shall be addressed to the Board's Executive
Secretary at the address below. The closing period for their receipt is
March 28, 2011. Rebuttal comments in response to material submitted
during the foregoing period may be submitted during the subsequent 15-
day period to April 11, 2011.
A copy of the application 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 https://www.trade.gov/ftz.
For further information, contact Diane Finver at
Diane.Finver@trade.gov or (202) 482-1367.
Dated: January 18, 2011.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2011-1506 Filed 1-24-11; 8:45 am]
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