Notice of Issuance of Final Determination Concerning Walkers, 64978-64979 [E8-25979]
Download as PDF
64978
Federal Register / Vol. 73, No. 212 / Friday, October 31, 2008 / Notices
proposes to test a high resolution, 360
degree field-of-view video system that
will accommodate multiple
simultaneous users and also have
change detection and tracking
capabilities. A PIA is being conducted
because the system demonstration will
be performed in a public area of New
York City and will involve capturing
images of persons and textual
information in the public space.
System: Department of Homeland
Security General Contact List.
Component: DHS Wide.
Date of approval: June 30, 2008.
Many Department of Homeland
Security operations and projects collect
a minimal amount of contact
information in order to distribute
information and perform various other
administrative tasks. Department
Headquarters conducted this privacy
impact assessment because contact lists
contain PII. The Department added the
following systems to this PIA:
• Science and Technology Cyber
Security Research and Development
Center Web Site,
• U.S. Coast Guard Proceedings
magazine online subscription request
form,
• Federal Emergency Management
Agency National Fire Academy LongTerm Evaluation,
• Federal Emergency Management
Agency Port Security Grant Program,
• National Protection and Programs
Directorate Telecommunications Service
Priority (TSP) Web.
Dated: October 21, 2008.
Hugo Teufel III,
Chief Privacy Officer, Department of
Homeland Security.
[FR Doc. E8–25962 Filed 10–30–08; 8:45 am]
BILLING CODE 4410–10–P
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
Notice of Issuance of Final
Determination Concerning Walkers
Dated: October 22, 2008.
Sandra L. Bell,
Executive Director, Office of Regulations and
Rulings, Office of International Trade.
Attachment
U.S. Customs and Border
Protection, Department of Homeland
Security.
ACTION: Notice of final determination.
ebenthall on PROD1PC60 with NOTICES
AGENCY:
SUMMARY: This document provides
notice that U.S. Customs and Border
Protection (‘‘CBP’’) has issued a final
determination concerning the country of
origin of certain walkers which may be
offered to the United States Government
under a government procurement
contract. Based upon the facts
presented, in the final determination
VerDate Aug<31>2005
15:31 Oct 30, 2008
Jkt 217001
CBP concluded that Hong Kong is the
country of origin of the walkers for
purposes of U.S. Government
procurement.
DATES: The final determination was
issued on October 22, 2008. A copy of
the final determination is attached. Any
party-at-interest, as defined in 19 CFR
177.22(d), may seek judicial review of
this final determination within
December 1, 2008.
FOR FURTHER INFORMATION CONTACT:
Gerry O’Brien, Valuation and Special
Programs Branch, Regulations and
Rulings, Office of International Trade
(202–572–8792).
SUPPLEMENTARY INFORMATION: Notice is
hereby given that on October 22, 2008,
pursuant to subpart B of part 177,
Customs Regulations (19 CFR part 177,
subpart B), CBP issued a final
determination concerning the country of
origin of certain walkers which may be
offered to the United States Government
under a government procurement
contract. This final determination, in
HQ H033839, was issued at the request
of Drive Medical Design and
Manufacturing under procedures set
forth at 19 CFR part 177, subpart B,
which implements Title III of the Trade
Agreements Act of 1979, as amended
(19 U.S.C. 2511–18). In the final
determination, CBP concluded that,
based upon the facts presented, certain
articles will be substantially
transformed in Hong Kong. Therefore,
CBP found that Hong Kong is the
country of origin of the finished articles
for purposes of U.S. Government
procurement.
Section 177.29, Customs Regulations
(19 CFR 177.29), provides that notice of
final determinations shall be published
in the Federal Register within 60 days
of the date the final determination is
issued. Section 177.30, CBP Regulations
(19 CFR 177.30), provides that any
party-at-interest, as defined in 19 CFR
177.22(d), may seek judicial review of a
final determination within 30 days of
publication of such determination in the
Federal Register.
HQ H033839
October 22, 2008
MAR–2–05 OT:RR:CTF:VS H033839 GOB
Category: Marking. Beth C. Ring, Esq.,
Sandler, Travis & Rosenberg, P.A., 551
Fifth Avenue, New York, NY 10176.
Re: U.S. Government Procurement; Title III,
Trade Agreements Act of 1979 (19 U.S.C.
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
2511); Subpart B, Part 177, CBP
Regulations; Walkers
Dear Ms. Ring: This is in response to your
letter of July 18, 2008, requesting a final
determination on behalf of Drive Medical
Design and Manufacturing (‘‘Drive Medical’’),
pursuant to subpart B of Part 177, Customs
and Border Protection (‘‘CBP’’) Regulations
(19 CFR 177.21 et seq.). You made a
supplemental submission on September 29,
2008. Under the pertinent regulations, which
implement Title III of the Trade Agreements
Act of 1979, as amended (19 U.S.C. 2511 et
seq.), CBP issues country of origin advisory
rulings and final determinations as to
whether an article is or would be a product
of a designated country or instrumentality for
the purpose of granting waivers of certain
‘‘Buy American’’ restrictions in U.S. law or
practice for products offered for sale to the
U.S. Government.
This final determination concerns the
country of origin of certain walkers. We note
that Drive Medical is a party-at-interest
within the meaning of 19 CFR 177.22(d)(1)
and is entitled to request this final
determination.
Facts
You describe the pertinent facts as follows.
Drive Medical will assemble the walkers at
a facility in Hong Kong. You state that the
two ‘‘U’’ frame side pieces will be
manufactured in Hong Kong. All of the other
parts will be manufactured in China. The
parts consist of the following:
• two ‘‘U’’ frame side pieces
• two release pins
• two springs
• four brass pins
• four stainless steel wire springs
• four crossbars
• one ‘‘H’’ frame
• four silencer caps
• four rubber tips
• two composite plastic hand grips
• two plastic push buttons
• an assortment of steel screws and nuts
You describe the manufacturing process as
follows:
• The side frame is fitted with a handle
grip using high pressure air to seat the handle
in the proper position, The handle grip is
heated prior to this process for better
malleability.
• The top cross brace is secured to the side
frame using a stainless steel star nut applied
with an air screwdriver with a predetermined
torque setting. This process is carried out on
both front and back of the side frame and on
both the left and right side.
• The side frames are placed through the
ends of the center ‘‘H’’ frame. During this
process a silencer ring is placed on the
bottom tubes of the ‘‘H’’ frame, and an
internal spacer is wrapped on the inside of
the top of the ‘‘H’’ frame to reduce ‘‘wobble.’’
• A rivet with plastic guide is now
mounted under the ‘‘H’’ frame directly to the
side frame on both sides. These rivets hold
the ‘‘H’’ frame in place.
• The lower side ‘‘U’’ frame support is
now riveted to the side frame, front and back,
on both sides of the walker.
• Release pins are dropped into both sides
of the ‘‘H’’ frame to create the folding
E:\FR\FM\31OCN1.SGM
31OCN1
Federal Register / Vol. 73, No. 212 / Friday, October 31, 2008 / Notices
mechanism catch. A spring and ‘‘C’’ clamp
are added to the release pin on both sides of
the walker.
• A flat folding guide plate is riveted to
both sides on top of the release pins. Two
rivets are used to secure the plate. One rivet
is used to secure the side frame. The other
is used to secure the folding guide plate to
the ‘‘H’’ frame.
• The rivet that holds the flat folding guide
plate to the ‘‘H’’ frame is outfitted with a
plastic guide washer by placing the guide
washer over the rivet during installation.
This process allows for smooth operation
when opening and folding the walker. The
rivet is calibrated in tension for smooth
operation and to reduce ‘‘wobble.’’
• A plastic release button is riveted to the
flat folding guide that initiates the folding
mechanism. Pushing the plastic release
activates the release pin.
• The rivet that secures the plastic release
pad is calibrated to ensure a positive ‘‘click’’
when securely opened and for easy
functioning.
• Four brass buttons are inserted into the
four legs of the side frames. The brass buttons
are inserted into the leg of the walker. A wire
spring is added to the button before insertion.
• Four anti-rattle bushings are pressed and
hammered to the bottom of each side frame
leg.
• A silencer cap and tip are pressed and
hammered to each external adjustable height
leg and assembled to the walker.
• A rubber tip is heated in this process to
ensure a snug fit.
• The legs are attached to the walker to
ensure the proper fit and are then removed
for shipping.
• Operation stickers and manuals are
added to the walker.
• The walker is individually bagged, boxed
and shipped.
You further state as follows. The walker is
manufactured to Drive Medical’s
specifications in order to impart
characteristics of strength, durability, and
flexibility. The design of the front cross frame
was developed in the U.S. The calibration of
the opening and closing mechanism is
important to the operation of the walker in
that it is essential that the user of the walker
be able to open and close it with little effort.
You state that the cost of the two ‘‘U’’ frame
side pieces is approximately 52 percent of
the total cost of the components and the cost
of manufacturing in Hong Kong (including
the cost of the two ‘‘U’’ frame side pieces) is
70 to 80 percent of the total cost of the
walker.
ebenthall on PROD1PC60 with NOTICES
Issue
What is the country of origin of the subject
walkers for the purpose of U.S. Government
procurement?
Law and Analysis
Pursuant to Subpart B of Part 177, 19 CFR
177.21 et seq., which implements Title III of
the Trade Agreements Act of 1979, as
amended (19 U.S.C. 2511 et seq.), CBP issues
country of origin advisory rulings and final
determinations as to whether an article is or
would be a product of a designated country
or instrumentality for the purposes of
VerDate Aug<31>2005
15:31 Oct 30, 2008
Jkt 217001
granting waivers of certain ‘‘Buy American’’
restrictions in U.S. law or practice for
products offered for sale to the U.S.
Government.
Under the rule of origin set forth under 19
U.S.C. 2518(4)(B):
An article is a product of a country or
instrumentality only if (i) it is wholly the
growth, product, or manufacture of that
country or instrumentality, or (ii) in the case
of an article which consists in whole or in
part of materials from another country or
instrumentality, it has been substantially
transformed into a new and different article
of commerce with a name, character, or use
distinct from that of the article or articles
from which it was so transformed.
See also, 19 CFR 177.22(a).
In rendering advisory rulings and final
determinations for purposes of U.S.
Government procurement, CBP applies the
provisions of subpart B of Part 177 consistent
with the Federal Procurement Regulations.
See 19 CFR 177.21. In this regard, CBP
recognizes that the Federal Procurement
Regulations restrict the U.S. Government’s
purchase of products to U.S.-made or
designated country end products for
acquisitions subject to the TAA. See 48 CFR
25.403(c)(1). The Federal Procurement
Regulations define ‘‘U.S.-made end product’’
as:
* * * an article that is mined, produced,
or manufactured in the United States or that
is substantially transformed in the United
States into a new and different article of
commerce with a name, character, or use
distinct from that of the article or articles
from which it was transformed.
48 CFR 25.003.
In determining whether the combining of
parts or materials constitutes a substantial
transformation, the determinative issue is the
extent of operations performed and whether
the parts lose their identity and become an
integral part of the new article. Belcrest
Linens v. United States, 573 F. Supp. 1149
(Ct. Int’l Trade 1983), aff’d, 741 F.2d 1368
(Fed. Cir. 1984). Assembly operations that are
minimal or simple, as opposed to complex or
meaningful, will generally not result in a
substantial transformation. See, C.S.D. 80–
111, C.S.D. 85–25, C.S.D. 89–110, C.S.D. 89–
118, C.S.D. 90–51, and C.S.D. 90–97. If the
manufacturing or combining process is a
minor one which leaves the identity of the
article intact, a substantial transformation has
not occurred. Uniroyal, Inc. v. United States,
3 CIT 220, 542 F. Supp. 1026 (1982), aff’d
702 F. 2d 1022 (Fed. Cir. 1983). In Uniroyal,
the court determined that a substantial
transformation did not occur when an
imported upper, the essence of the finished
article, was combined with a domestically
produced outsole to form a shoe.
In order to determine whether a substantial
transformation occurs when components of
various origins are assembled into completed
products, CBP considers the totality of the
circumstances and makes such
determinations on a case-by-case basis. The
country of origin of the item’s components,
extent of the processing that occurs within a
country, and whether such processing
renders a product with a new name,
PO 00000
Frm 00073
Fmt 4703
Sfmt 4703
64979
character, and use are primary considerations
in such cases. Additionally, factors such as
the resources expended on product design
and development, extent and nature of postassembly inspection and testing procedures,
and the degree of skill required during the
actual manufacturing process may be
relevant when determining whether a
substantial transformation has occurred. No
one factor is determinative.
You cite HQ H017620, dated February 5,
2008, where CBP held that certain imported
components of a flashlight and replacement
lens head subassembly were substantially
transformed as a result of manufacturing
operations in the U.S. In that ruling, CBP
stated:
In support of this conclusion, we agree that
the U.S.-origin LED imparts the essential
character to both the replacement part and
the finished product, as it generates the
primary light of both products. We also
recognize that Energizer has expended
significant resources in connection with the
design and development of the subject
flashlight in the United States. Moreover, the
U.S.-origin LED and the labor performed in
the United States during the assembly and
testing operations represent a majority of the
costs associated with the production of both
the replacement lens head subassembly and
the finished flashlight.
After a consideration of the evidence of
record, we find that the operations in Hong
Kong, including the manufacture in Hong
Kong of the two ‘‘U’’ side frame pieces, will
result in a substantial transformation of the
components imported into Hong Kong. In
making this finding, we note that all of the
assembly operations will occur in Hong Kong
and that the two ‘‘U’’ side frame pieces,
which are manufactured in Hong Kong, are
extremely vital parts of the walkers.
Based upon this finding, we determine that
the country of origin of the walkers for the
purpose of government procurement is Hong
Kong.
Holding
The operations to be performed in Hong
Kong will result in a substantial
transformation of the goods imported into
Hong Kong from China. Therefore, the
country of origin of the walkers for the
purpose of government procurement is Hong
Kong.
Notice of this final determination will be
given in the Federal Register, as required by
19 CFR 177.29. Any party-at-interest other
than the party which requested this final
determination may request, pursuant to 19
CFR 177.31, that CBP reexamine the matter
anew and issue a new final determination.
Pursuant to 19 CFR 177.30, any party-atinterest may, within 30 days after publication
of the Federal Register notice referenced
above, seek judicial review of this final
determination before the Court of
International Trade.
Sincerely,
Sandra L. Bell
Executive Director
Office of Regulations and Rulings
Office of International Trade.
[FR Doc. E8–25979 Filed 10–30–08; 8:45 am]
BILLING CODE 9111–14–P
E:\FR\FM\31OCN1.SGM
31OCN1
Agencies
[Federal Register Volume 73, Number 212 (Friday, October 31, 2008)]
[Notices]
[Pages 64978-64979]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-25979]
-----------------------------------------------------------------------
DEPARTMENT OF HOMELAND SECURITY
U.S. Customs and Border Protection
Notice of Issuance of Final Determination Concerning Walkers
AGENCY: U.S. Customs and Border Protection, Department of Homeland
Security.
ACTION: Notice of final determination.
-----------------------------------------------------------------------
SUMMARY: This document provides notice that U.S. Customs and Border
Protection (``CBP'') has issued a final determination concerning the
country of origin of certain walkers which may be offered to the United
States Government under a government procurement contract. Based upon
the facts presented, in the final determination CBP concluded that Hong
Kong is the country of origin of the walkers for purposes of U.S.
Government procurement.
DATES: The final determination was issued on October 22, 2008. A copy
of the final determination is attached. Any party-at-interest, as
defined in 19 CFR 177.22(d), may seek judicial review of this final
determination within December 1, 2008.
FOR FURTHER INFORMATION CONTACT: Gerry O'Brien, Valuation and Special
Programs Branch, Regulations and Rulings, Office of International Trade
(202-572-8792).
SUPPLEMENTARY INFORMATION: Notice is hereby given that on October 22,
2008, pursuant to subpart B of part 177, Customs Regulations (19 CFR
part 177, subpart B), CBP issued a final determination concerning the
country of origin of certain walkers which may be offered to the United
States Government under a government procurement contract. This final
determination, in HQ H033839, was issued at the request of Drive
Medical Design and Manufacturing under procedures set forth at 19 CFR
part 177, subpart B, which implements Title III of the Trade Agreements
Act of 1979, as amended (19 U.S.C. 2511-18). In the final
determination, CBP concluded that, based upon the facts presented,
certain articles will be substantially transformed in Hong Kong.
Therefore, CBP found that Hong Kong is the country of origin of the
finished articles for purposes of U.S. Government procurement.
Section 177.29, Customs Regulations (19 CFR 177.29), provides that
notice of final determinations shall be published in the Federal
Register within 60 days of the date the final determination is issued.
Section 177.30, CBP Regulations (19 CFR 177.30), provides that any
party-at-interest, as defined in 19 CFR 177.22(d), may seek judicial
review of a final determination within 30 days of publication of such
determination in the Federal Register.
Dated: October 22, 2008.
Sandra L. Bell,
Executive Director, Office of Regulations and Rulings, Office of
International Trade.
Attachment
HQ H033839
October 22, 2008
MAR-2-05 OT:RR:CTF:VS H033839 GOB
Category: Marking. Beth C. Ring, Esq., Sandler, Travis & Rosenberg,
P.A., 551 Fifth Avenue, New York, NY 10176.
Re: U.S. Government Procurement; Title III, Trade Agreements Act of
1979 (19 U.S.C. 2511); Subpart B, Part 177, CBP Regulations; Walkers
Dear Ms. Ring: This is in response to your letter of July 18,
2008, requesting a final determination on behalf of Drive Medical
Design and Manufacturing (``Drive Medical''), pursuant to subpart B
of Part 177, Customs and Border Protection (``CBP'') Regulations (19
CFR 177.21 et seq.). You made a supplemental submission on September
29, 2008. Under the pertinent regulations, which implement Title III
of the Trade Agreements Act of 1979, as amended (19 U.S.C. 2511 et
seq.), CBP issues country of origin advisory rulings and final
determinations as to whether an article is or would be a product of
a designated country or instrumentality for the purpose of granting
waivers of certain ``Buy American'' restrictions in U.S. law or
practice for products offered for sale to the U.S. Government.
This final determination concerns the country of origin of
certain walkers. We note that Drive Medical is a party-at-interest
within the meaning of 19 CFR 177.22(d)(1) and is entitled to request
this final determination.
Facts
You describe the pertinent facts as follows. Drive Medical will
assemble the walkers at a facility in Hong Kong. You state that the
two ``U'' frame side pieces will be manufactured in Hong Kong. All
of the other parts will be manufactured in China. The parts consist
of the following:
two ``U'' frame side pieces
two release pins
two springs
four brass pins
four stainless steel wire springs
four crossbars
one ``H'' frame
four silencer caps
four rubber tips
two composite plastic hand grips
two plastic push buttons
an assortment of steel screws and nuts
You describe the manufacturing process as follows:
The side frame is fitted with a handle grip using high
pressure air to seat the handle in the proper position, The handle
grip is heated prior to this process for better malleability.
The top cross brace is secured to the side frame using
a stainless steel star nut applied with an air screwdriver with a
predetermined torque setting. This process is carried out on both
front and back of the side frame and on both the left and right
side.
The side frames are placed through the ends of the
center ``H'' frame. During this process a silencer ring is placed on
the bottom tubes of the ``H'' frame, and an internal spacer is
wrapped on the inside of the top of the ``H'' frame to reduce
``wobble.''
A rivet with plastic guide is now mounted under the
``H'' frame directly to the side frame on both sides. These rivets
hold the ``H'' frame in place.
The lower side ``U'' frame support is now riveted to
the side frame, front and back, on both sides of the walker.
Release pins are dropped into both sides of the ``H''
frame to create the folding
[[Page 64979]]
mechanism catch. A spring and ``C'' clamp are added to the release
pin on both sides of the walker.
A flat folding guide plate is riveted to both sides on
top of the release pins. Two rivets are used to secure the plate.
One rivet is used to secure the side frame. The other is used to
secure the folding guide plate to the ``H'' frame.
The rivet that holds the flat folding guide plate to
the ``H'' frame is outfitted with a plastic guide washer by placing
the guide washer over the rivet during installation. This process
allows for smooth operation when opening and folding the walker. The
rivet is calibrated in tension for smooth operation and to reduce
``wobble.''
A plastic release button is riveted to the flat folding
guide that initiates the folding mechanism. Pushing the plastic
release activates the release pin.
The rivet that secures the plastic release pad is
calibrated to ensure a positive ``click'' when securely opened and
for easy functioning.
Four brass buttons are inserted into the four legs of
the side frames. The brass buttons are inserted into the leg of the
walker. A wire spring is added to the button before insertion.
Four anti-rattle bushings are pressed and hammered to
the bottom of each side frame leg.
A silencer cap and tip are pressed and hammered to each
external adjustable height leg and assembled to the walker.
A rubber tip is heated in this process to ensure a snug
fit.
The legs are attached to the walker to ensure the
proper fit and are then removed for shipping.
Operation stickers and manuals are added to the walker.
The walker is individually bagged, boxed and shipped.
You further state as follows. The walker is manufactured to
Drive Medical's specifications in order to impart characteristics of
strength, durability, and flexibility. The design of the front cross
frame was developed in the U.S. The calibration of the opening and
closing mechanism is important to the operation of the walker in
that it is essential that the user of the walker be able to open and
close it with little effort. You state that the cost of the two
``U'' frame side pieces is approximately 52 percent of the total
cost of the components and the cost of manufacturing in Hong Kong
(including the cost of the two ``U'' frame side pieces) is 70 to 80
percent of the total cost of the walker.
Issue
What is the country of origin of the subject walkers for the
purpose of U.S. Government procurement?
Law and Analysis
Pursuant to Subpart B of Part 177, 19 CFR 177.21 et seq., which
implements Title III of the Trade Agreements Act of 1979, as amended
(19 U.S.C. 2511 et seq.), CBP issues country of origin advisory
rulings and final determinations as to whether an article is or
would be a product of a designated country or instrumentality for
the purposes of granting waivers of certain ``Buy American''
restrictions in U.S. law or practice for products offered for sale
to the U.S. Government.
Under the rule of origin set forth under 19 U.S.C. 2518(4)(B):
An article is a product of a country or instrumentality only if
(i) it is wholly the growth, product, or manufacture of that country
or instrumentality, or (ii) in the case of an article which consists
in whole or in part of materials from another country or
instrumentality, it has been substantially transformed into a new
and different article of commerce with a name, character, or use
distinct from that of the article or articles from which it was so
transformed.
See also, 19 CFR 177.22(a).
In rendering advisory rulings and final determinations for
purposes of U.S. Government procurement, CBP applies the provisions
of subpart B of Part 177 consistent with the Federal Procurement
Regulations. See 19 CFR 177.21. In this regard, CBP recognizes that
the Federal Procurement Regulations restrict the U.S. Government's
purchase of products to U.S.-made or designated country end products
for acquisitions subject to the TAA. See 48 CFR 25.403(c)(1). The
Federal Procurement Regulations define ``U.S.-made end product'' as:
* * * an article that is mined, produced, or manufactured in the
United States or that is substantially transformed in the United
States into a new and different article of commerce with a name,
character, or use distinct from that of the article or articles from
which it was transformed.
48 CFR 25.003.
In determining whether the combining of parts or materials
constitutes a substantial transformation, the determinative issue is
the extent of operations performed and whether the parts lose their
identity and become an integral part of the new article. Belcrest
Linens v. United States, 573 F. Supp. 1149 (Ct. Int'l Trade 1983),
aff'd, 741 F.2d 1368 (Fed. Cir. 1984). Assembly operations that are
minimal or simple, as opposed to complex or meaningful, will
generally not result in a substantial transformation. See, C.S.D.
80-111, C.S.D. 85-25, C.S.D. 89-110, C.S.D. 89-118, C.S.D. 90-51,
and C.S.D. 90-97. If the manufacturing or combining process is a
minor one which leaves the identity of the article intact, a
substantial transformation has not occurred. Uniroyal, Inc. v.
United States, 3 CIT 220, 542 F. Supp. 1026 (1982), aff'd 702 F. 2d
1022 (Fed. Cir. 1983). In Uniroyal, the court determined that a
substantial transformation did not occur when an imported upper, the
essence of the finished article, was combined with a domestically
produced outsole to form a shoe.
In order to determine whether a substantial transformation
occurs when components of various origins are assembled into
completed products, CBP considers the totality of the circumstances
and makes such determinations on a case-by-case basis. The country
of origin of the item's components, extent of the processing that
occurs within a country, and whether such processing renders a
product with a new name, character, and use are primary
considerations in such cases. Additionally, factors such as the
resources expended on product design and development, extent and
nature of post-assembly inspection and testing procedures, and the
degree of skill required during the actual manufacturing process may
be relevant when determining whether a substantial transformation
has occurred. No one factor is determinative.
You cite HQ H017620, dated February 5, 2008, where CBP held that
certain imported components of a flashlight and replacement lens
head subassembly were substantially transformed as a result of
manufacturing operations in the U.S. In that ruling, CBP stated:
In support of this conclusion, we agree that the U.S.-origin LED
imparts the essential character to both the replacement part and the
finished product, as it generates the primary light of both
products. We also recognize that Energizer has expended significant
resources in connection with the design and development of the
subject flashlight in the United States. Moreover, the U.S.-origin
LED and the labor performed in the United States during the assembly
and testing operations represent a majority of the costs associated
with the production of both the replacement lens head subassembly
and the finished flashlight.
After a consideration of the evidence of record, we find that
the operations in Hong Kong, including the manufacture in Hong Kong
of the two ``U'' side frame pieces, will result in a substantial
transformation of the components imported into Hong Kong. In making
this finding, we note that all of the assembly operations will occur
in Hong Kong and that the two ``U'' side frame pieces, which are
manufactured in Hong Kong, are extremely vital parts of the walkers.
Based upon this finding, we determine that the country of origin
of the walkers for the purpose of government procurement is Hong
Kong.
Holding
The operations to be performed in Hong Kong will result in a
substantial transformation of the goods imported into Hong Kong from
China. Therefore, the country of origin of the walkers for the
purpose of government procurement is Hong Kong.
Notice of this final determination will be given in the Federal
Register, as required by 19 CFR 177.29. Any party-at-interest other
than the party which requested this final determination may request,
pursuant to 19 CFR 177.31, that CBP reexamine the matter anew and
issue a new final determination. Pursuant to 19 CFR 177.30, any
party-at-interest may, within 30 days after publication of the
Federal Register notice referenced above, seek judicial review of
this final determination before the Court of International Trade.
Sincerely,
Sandra L. Bell
Executive Director
Office of Regulations and Rulings
Office of International Trade.
[FR Doc. E8-25979 Filed 10-30-08; 8:45 am]
BILLING CODE 9111-14-P