Foreign-Trade Zone (FTZ) 43-Battle Creek, Michigan; Notification of Proposed Production Activity; Pfizer, Inc. (mRNA COVID-19 Vaccine); Kalamazoo, Michigan, 46177-46178 [2021-17692]
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Federal Register / Vol. 86, No. 157 / Wednesday, August 18, 2021 / Notices
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within New South Wales District),
subject to the following phytosanitary
measures:
• The citrus must either originate
from an area within these approved
production areas that is free of the fruit
flies Queensland fruit fly, Medfly, and/
or Bactrocera neohumeralis (Lesser
Queensland fruit fly), or be treated with
cold treatment or other approved
treatment for the relevant fruit flies.
• If the area has Queensland fruit fly
or Lesser Queensland fruit fly, cold
treatment schedules T107–d–2 or T107–
d–3 must be used.
• The citrus fruit must be
accompanied by a phytosanitary
certificate issued by the NPPO of
Australia that attests that citrus fruit
were produced in a fruit fly pest-free
area or that indicates that cold treatment
was applied to the consignment during
transit to the continental United States,
or a combination of PFAs and
quarantine treatments; were inspected
by the NPPO of Australia and found free
of pests of concern. We are not requiring
an additional declaration for light
brown apple moth because the PRA
considers this pest unlikely to follow
the pathway on citrus fruit from these
areas.
• The citrus fruit is subject to
inspection at the port of entry into the
United States.
• Only commercial consignments of
Australian citrus fruit may be imported
into the United States.
• Fruit must be washed, brushed,
surface disinfected in accordance with 7
CFR part 305 and according to treatment
schedules listed in the USDA Treatment
Manual, treated with fungicide at
labeled rates, and waxed at
packinghouses.
• An operational work plan that
details the requirements under which
citrus will be safely imported is in
place.
• The citrus fruit must be imported
under permit.
These revised conditions will be
listed in the FAVIR database (available
at https://epermits.aphis.usda.gov/
manual). In addition to these specific
measures, citrus from Australia will be
subject to the general requirements
listed in § 319.56–3 that are applicable
to the importation of all fruits and
vegetables.
Paperwork Reduction Act
In accordance with the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501
et seq.), the burden requirements
associated with this action are included
under the Office of Management and
Budget control number 0579–0049.
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E-Government Act Compliance
The Animal and Plant Health
Inspection Service is committed to
compliance with the E-Government Act
to promote the use of the internet and
other information technologies, to
provide increased opportunities for
citizen access to Government
information and services, and for other
purposes. For information pertinent to
E-Government Act compliance related
to this notice, please contact Mr. Joseph
Moxey, APHIS’ Paperwork Reduction
Act Coordinator, at (301) 851–2483.
Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), the Office of
Information and Regulatory Affairs
designated this action as not a major
rule, as defined by 5 U.S.C. 804(2).
Authority: 7 U.S.C. 1633, 7701–7772,
and 7781–7786; 21 U.S.C. 136 and 136a;
7 CFR 2.22, 2.80, and 371.3.
Done in Washington, DC, this 12th day of
August 2021.
Mark Davidson,
Acting Administrator, Animal and Plant
Health Inspection Service.
[FR Doc. 2021–17709 Filed 8–17–21; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–29–2021]
Foreign-Trade Zone (FTZ) 107—Des
Moines, Iowa; Authorization of
Production Activity; Lely North
America, Inc. (Automated Milking and
Feeding Equipment); Pella, Iowa
On April 14, 2021, Lely North
America, Inc. (Lely) submitted a
notification of proposed production
activity to the FTZ Board for its facility
within Subzone 107E, in Pella, Iowa.
The notification was processed in
accordance with the regulations of the
FTZ Board (15 CFR part 400), including
notice in the Federal Register inviting
public comment (86 FR 21686, April 23,
2021). On August 12, 2021, the
applicant was notified of the FTZ
Board’s decision that no further review
of the activity is warranted at this time.
The production activity described in the
notification was authorized, subject to
the FTZ Act and the FTZ Board’s
regulations, including Section 400.14.
Dated: August 12, 2021.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2021–17691 Filed 8–17–21; 8:45 am]
BILLING CODE 3510–DS–P
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46177
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–58–2021]
Foreign-Trade Zone (FTZ) 43—Battle
Creek, Michigan; Notification of
Proposed Production Activity; Pfizer,
Inc. (mRNA COVID–19 Vaccine);
Kalamazoo, Michigan
Pfizer, Inc. (Pfizer) submitted a
notification of proposed production
activity to the FTZ Board for its
facilities in Kalamazoo, Michigan. The
notification conforming to the
requirements of the regulations of the
FTZ Board (15 CFR 400.22) was
received on August 6, 2021.
Pfizer already has authority to
produce pharmaceutical, consumer
healthcare and animal healthcare
products within Subzone 43E. The
current request would add a finished
product and a foreign-status material/
component to the scope of authority.
Pursuant to 15 CFR 400.14(b),
additional FTZ authority would be
limited to the specific foreign-status
material/component and specific
finished product described in the
submitted notification (as described
below) and subsequently authorized by
the FTZ Board.
Production under FTZ procedures
could exempt Pfizer from customs duty
payments on the foreign-status material/
component used in export production.
On its domestic sales, for the foreignstatus material/component noted below
and in the existing scope of authority,
Pfizer would be able to choose the duty
rate during customs entry procedures
that applies to the mRNA COVID–19
vaccine (duty-free). Pfizer would be able
to avoid duty on foreign-status
components which become scrap/waste.
Customs duties also could possibly be
deferred or reduced on foreign-status
production equipment.
The proposed foreign-status material/
component is mRNA bulk drug
substance (duty rate—6.5%). The
company currently intends to ship
mRNA bulk drug substance produced at
its facility in Andover, Massachusetts
(Subzone 27R) to its Kalamazoo
facilities for further processing.
Public comment is invited from
interested parties. Submissions shall be
addressed to the Board’s Executive
Secretary and sent to: ftz@trade.gov. The
closing period for their receipt is
September 27, 2021.
A copy of the notification will be
available for public inspection in the
‘‘Reading Room’’ section of the Board’s
website, which is accessible via
www.trade.gov/ftz.
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Federal Register / Vol. 86, No. 157 / Wednesday, August 18, 2021 / Notices
For further information, contact Diane
Finver at Diane.Finver@trade.gov.
Dated: August 12, 2021.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2021–17692 Filed 8–17–21; 8:45 am]
BILLING CODE 3510–DS–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–31–2021]
Foreign-Trade Zone (FTZ) 45—
Portland, Oregon; Authorization of
Production Activity; Lam Research
Corporation (Semiconductor
Production Equipment, Subassemblies
and Related Parts), Tualatin and
Sherwood, Oregon
On April 14, 2021, the Port of
Portland, grantee of FTZ 45, submitted
a notification of proposed production
activity to the FTZ Board on behalf of
Lam Research Corporation, within
Subzone 45H, in Tualatin and
Sherwood, Oregon.
The notification was processed in
accordance with the regulations of the
FTZ Board (15 CFR part 400), including
notice in the Federal Register inviting
public comment (86 FR 22387–22389,
April 28, 2021). On August 12, 2021, the
applicant was notified of the FTZ
Board’s decision that no further review
of the activity is warranted at this time.
The production activity described in the
notification was authorized, subject to
the FTZ Act and the FTZ Board’s
regulations, including Section 400.14.
Dated: August 12, 2021.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2021–17689 Filed 8–17–21; 8:45 am]
BILLING CODE 3510–DS–P
DEPARTMENT OF COMMERCE
International Trade Administration
[A–570–106]
Wooden Cabinets and Vanities and
Components Thereof From the
People’s Republic of China:
Preliminary Recission of Antidumping
Duty New Shipper Review; 2020
Enforcement and Compliance,
International Trade Administration,
Department of Commerce.
SUMMARY: The Department of Commerce
(Commerce) preliminarily determines
that Dalian Hualing Wood Co., Ltd.
(Hualing) does not qualify as a new
shipper and we are preliminarily
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AGENCY:
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rescinding this new shipper review
(NSR). We invite interested parties to
comment on this preliminary rescission.
DATES: Applicable August 18, 2021.
FOR FURTHER INFORMATION CONTACT:
Jacob Keller, AD/CVD Operations Office
I, Enforcement and Compliance,
International Trade Administration,
U.S. Department of Commerce, 1401
Constitution Avenue NW, Washington,
DC 20230; telephone: (202) 482–4849.
SUPPLEMENTARY INFORMATION:
Background
On April 21, 2020, we published in
the Federal Register an antidumping
duty order on wooden cabinets and
vanities and components thereof
(cabinets) from the People’s Republic of
China (China).1 On December 1, 2020,
Commerce initiated the antidumping
duty NSR of wooden cabinets from
China for the period of review, April 1,
2020, through September 30, 2020, for
Hualing.2 For additional background,
see the Preliminary Decision
Memorandum.3
Scope of the Order
The products covered by the Order
are wooden cabinets and vanities that
are for permanent installation
(including floor mounted, wall
mounted, ceiling hung or by attachment
of plumbing), and wooden components
thereof. For a complete description of
the scope of the Order, see the
Preliminary Decision Memorandum.4
Methodology
Commerce is conducting this review
in accordance with section 75l(a)(2)(B)
of the Tariff Act of 1930, as amended
(the Act), and 19 CFR 351.214. For a full
description of the methodology
underlying our conclusions, see the
Preliminary Decision Memorandum. A
list of sections in the Preliminary
Decision Memorandum is attached in
the appendix to this notice. The
Preliminary Decision Memorandum is a
public document and is made available
to the public via Enforcement and
Compliance’s Antidumping and
1 See Wooden Cabinets and Vanities and
Components Thereof from the People’s Republic of
China: Antidumping Duty Order, 86 FR 22126
(April 21, 2020) (Order).
2 See Wooden Cabinets and Vanities and
Components Thereof from the People’s Republic of
China: Initiation of Antidumping Duty New Shipper
Review, 85 FR 77162 (December 1, 2020).
3 See Memorandum, ‘‘Wooden Cabinets and
Vanities and Components Thereof from the People’s
Republic of China: Decision Memorandum for the
Preliminary Intent to Rescind the Antidumping
Duty New Shipper Review; 2020,’’ issued
concurrently with, and hereby adopted by, this
notice (Preliminary Decision Memorandum).
4 Id.
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Countervailing Duty Centralized
Electronic Service System (ACCESS).
ACCESS is available to registered users
at https://access.trade.gov. In addition, a
complete version of the Preliminary
Decision Memorandum can be accessed
directly at https://enforcement.trade.gov/
frn/.
Preliminary Intent To Rescind the
Antidumping Duty New Shipper
Review
Based on information on the record,
we determine that Hualing does not
meet the minimum requirements in its
request for the NSR under 19 CFR
351.214(b)(2)(i). Therefore, we
preliminarily determine that it is
appropriate to rescind the NSR with
respect to Hualing.5
Public Comment
Pursuant to 19 CFR 351.309(c)(1)(ii),
interested parties may submit case briefs
no later than 30 days after the date of
publication of this notice. Rebuttal
briefs, limited to issues raised in the
case briefs, may be filed no later than
seven days after the time limit for filing
case briefs.6 Commerce has modified
certain of its requirements for serving
documents containing business
proprietary information until further
notice.7 Parties who submit case briefs
or rebuttal briefs in this proceeding are
requested to submit with each brief: (1)
A statement of the issue; (2) a brief
summary of the argument; and (3) a
table of authorities.8 Executive
summaries should be limited to five
pages total, including footnotes.9 All
submissions, with limited exceptions,
must be filed electronically using
ACCESS.10 Electronically filed
comments must be received successfully
in its entirety by Commerce’s electronic
records system, ACCESS, by 5 p.m.
Eastern Time on the due date.
Pursuant to 19 CFR 351.310(c),
interested parties who wish to request a
hearing, must submit a written request
to the Assistant Secretary for
Enforcement and Compliance, filed
electronically via ACCESS. Requests
should contain: (1) The party’s name,
address, and telephone number; (2) the
number of participants; and (3) a list of
5 We have not conducted a detailed bona fides
analysis for these preliminary results due to the
preliminary decision that Hualing is not eligible for
an NSR. See the Preliminary Decision
Memorandum.
6 See 19 CFR 351.309(d)(1); see also Temporary
Rule Modifying AD/CVD Service Requirements Due
to COVID–19; Extension of Effective Period, 85 FR
41363 (July 10, 2020) (Temporary Rule).
7 See Temporary Rule.
8 See 19 CFR 351.309(c)(2) and (d)(2).
9 Id.
10 See 19 CFR 351.303.
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Agencies
[Federal Register Volume 86, Number 157 (Wednesday, August 18, 2021)]
[Notices]
[Pages 46177-46178]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-17692]
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DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B-58-2021]
Foreign-Trade Zone (FTZ) 43--Battle Creek, Michigan; Notification
of Proposed Production Activity; Pfizer, Inc. (mRNA COVID-19 Vaccine);
Kalamazoo, Michigan
Pfizer, Inc. (Pfizer) submitted a notification of proposed
production activity to the FTZ Board for its facilities in Kalamazoo,
Michigan. The notification conforming to the requirements of the
regulations of the FTZ Board (15 CFR 400.22) was received on August 6,
2021.
Pfizer already has authority to produce pharmaceutical, consumer
healthcare and animal healthcare products within Subzone 43E. The
current request would add a finished product and a foreign-status
material/component to the scope of authority. Pursuant to 15 CFR
400.14(b), additional FTZ authority would be limited to the specific
foreign-status material/component and specific finished product
described in the submitted notification (as described below) and
subsequently authorized by the FTZ Board.
Production under FTZ procedures could exempt Pfizer from customs
duty payments on the foreign-status material/component used in export
production. On its domestic sales, for the foreign-status material/
component noted below and in the existing scope of authority, Pfizer
would be able to choose the duty rate during customs entry procedures
that applies to the mRNA COVID-19 vaccine (duty-free). Pfizer would be
able to avoid duty on foreign-status components which become scrap/
waste. Customs duties also could possibly be deferred or reduced on
foreign-status production equipment.
The proposed foreign-status material/component is mRNA bulk drug
substance (duty rate--6.5%). The company currently intends to ship mRNA
bulk drug substance produced at its facility in Andover, Massachusetts
(Subzone 27R) to its Kalamazoo facilities for further processing.
Public comment is invited from interested parties. Submissions
shall be addressed to the Board's Executive Secretary and sent to:
[email protected]. The closing period for their receipt is September 27,
2021.
A copy of the notification will be available for public inspection
in the ``Reading Room'' section of the Board's website, which is
accessible via www.trade.gov/ftz.
[[Page 46178]]
For further information, contact Diane Finver at
[email protected].
Dated: August 12, 2021.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2021-17692 Filed 8-17-21; 8:45 am]
BILLING CODE 3510-DS-P