Notice of Request for Revision of an Approved Information Collection (Consumer Complaint Monitoring System)

Published date19 March 2021
Citation86 FR 14865
Record Number2021-05734
SectionNotices
CourtFood Safety And Inspection Service
This section of the FEDERAL REGISTER
contains documents other than rules or
proposed rules that are applicable to the
public. Notices of hearings and investigations,
committee meetings, agency decisions and
rulings, delegations of authority, filing of
petitions and applications and agency
statements of organization and functions are
examples of documents appearing in this
section.
Notices Federal Register
14865
Vol. 86, No. 52
Friday, March 19, 2021
DEPARTMENT OF AGRICULTURE
Submission for OMB Review;
Comment Request
March 16, 2021.
The Department of Agriculture has
submitted the following information
collection requirement(s) to OMB for
review and clearance under the
Paperwork Reduction Act of 1995,
Public Law 104–13. Comments are
requested regarding; whether the
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility; the accuracy of the
agency’s estimate of burden including
the validity of the methodology and
assumptions used; ways to enhance the
quality, utility and clarity of the
information to be collected; and ways to
minimize the burden of the collection of
information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Comments regarding this information
collection received by April 19, 2021
will be considered. Written comments
and recommendations for the proposed
information collection should be
submitted within 30 days of the
publication of this notice on the
following website www.reginfo.gov/
public/do/PRAMain. Find this
particular information collection by
selecting ‘‘Currently under 30-day
Review—Open for Public Comments’’ or
by using the search function.
An agency may not conduct or
sponsor a collection of information
unless the collection of information
displays a currently valid OMB control
number and the agency informs
potential persons who are to respond to
the collection of information that such
persons are not required to respond to
the collection of information unless it
displays a currently valid OMB control
number.
Food and Nutrition Service
Title: Supplemental Nutrition
Assistance Program Requirement for
National Directory of New Hires
Employment Verification.
OMB Control Number: 0584–0608.
Summary of Collection: This
collection is a revision of an expired
collection at 84 FR 11928. In 2016, an
Interim Final Rule titled ‘‘Supplemental
Nutrition Assistance Program:
Requirement for National Directory of
New Hires Employment Verification
and Annual Program Activity
Reporting,’’ was published in the
Federal Register. This rule codified
section 4013 of the Agricultural Act of
2014, requiring State agencies to access
employment data through the National
Directory of New Hires (NDNH) at the
time of certification, including
recertification, to determine eligibility
status and correct benefit amount for
SNAP applicants. The rule also
amended regulations to increase the
frequency of the requirement for State
agency submission of the Program
Activity Statement from an annual
requirement based on the State fiscal
year to a quarterly requirement.
Need and Use of the Information:
Supplemental Nutrition Assistance
Program (SNAP) regulations at 7 CFR
272.16 require that each State agency
must establish a system to compare
identifiable information about each
adult household member against data
from the U.S. Department of Health and
Human Services’ (HHS) National
Directory of New Hires (NDNH). This
comparison will be used to determine
the eligibility status of the household
and determine the correct benefit
amount the household should receive.
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 of the
proposed collection of information,
including the validity of the
methodology and assumptions that were
used; (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 those who are to
respond, including use of appropriate
automated, electronic, mechanical, or
other technological collection
techniques or other forms of information
technology.
Description of Respondents: State and
Local Government, Individuals and
Households.
Number of Respondents: 1,180,536.
Frequency of Responses: Reporting:
On occasion.
Total Burden Hours: 521,719.
Ruth Brown,
Departmental Information Collection
Clearance Officer.
[FR Doc. 2021–05699 Filed 3–18–21; 8:45 am]
BILLING CODE 3410–30–P
DEPARTMENT OF AGRICULTURE
Food Safety and Inspection Service
[Docket No. FSIS–2021–0005]
Notice of Request for Revision of an
Approved Information Collection
(Consumer Complaint Monitoring
System)
AGENCY
: Food Safety and Inspection
Service, USDA.
ACTION
: Notice and request for
comments.
SUMMARY
: In accordance with the
Paperwork Reduction Act of 1995 and
the Office of Management and Budget
(OMB) regulations, the Food Safety and
Inspection Service (FSIS) is announcing
its intention to revise the approved
information collection regarding its
Consumer Complaint Monitoring
System (CCMS) web portal. The Agency
has increased the burden estimate by
575 hours due to increased use of the
Agency’s updated, more user-friendly
web portal that supports more direct
communication. The approval for this
information collection will expire on
September 30, 2021.
DATES
: Submit comments on or before
May 18, 2021
ADDRESSES
: FSIS invites interested
persons to submit comments on this
Federal Register notice. Comments may
be submitted by one of the following
methods:
Federal eRulemaking Portal: This
website provides commenters the ability
to type short comments directly into the
comment field on the web page or to
attach a file for lengthier comments. Go
to http://www.regulations.gov. Follow
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14866
Federal Register / Vol. 86, No. 52 / Friday, March 19, 2021 / Notices
the on-line instructions at that site for
submitting comments.
Mail, including CD–ROMs, etc.:
Send to Docket Clerk, U.S. Department
of Agriculture, Food Safety and
Inspection Service, 1400 Independence
Avenue SW, Mailstop 3758,
Washington, DC 20250–3700.
Hand- or courier-delivered
submittals: Deliver to 1400
Independence Avenue SW, Washington,
DC 20250–3700.
Instructions: All items submitted by
mail or electronic mail must include the
Agency name and docket number FSIS–
2021–0005. Comments received in
response to this docket will be made
available for public inspection and
posted without change, including any
personal information, to http://
www.regulations.gov.
Docket: For access to background
documents or comments received, call
(202)205–0495 to schedule a time to
visit the FSIS Docket Room at 1400
Independence Avenue SW, Washington,
DC 20250–3700.
FOR FURTHER INFORMATION CONTACT
: Gina
Kouba, Office of Policy and Program
Development, Food Safety and
Inspection Service, USDA, 1400
Independence Avenue SW, Mailstop
3758, South Building, Washington, DC
20250–3700; (202) 720–5627.
SUPPLEMENTARY INFORMATION
:
Title: Consumer Complaint
Monitoring System.
OMB Number: 0583–0133.
Expiration Date of Approval: 9/30/
2021.
Type of Request: Revision of an
approved information collection.
Abstract: FSIS has been delegated the
authority to exercise the functions of the
Secretary (7 CFR 2.18, 2.53), as specified
in the Federal Meat Inspection Act
(FMIA) (21 U.S.C. 601, et seq.), the
Poultry Products Inspection Act (PPIA)
(21 U.S.C. 451, et seq.), and the Egg
Products Inspection Act (EPIA) (21
U.S.C. 1031, et seq.). These statutes
mandate that FSIS protect the public by
verifying that meat, poultry, and egg
products are safe, wholesome,
unadulterated, and properly labeled and
packaged.
FSIS is requesting a revision of the
approved information collection
regarding its Consumer Complaint
Monitoring System (CCMS) web portal.
The Agency has increased the burden
estimate by 575 hours due to increased
use of the Agency’s updated, more user-
friendly web portal that supports more
direct communication. The approval for
this information collection will expire
on September 30, 2021.
FSIS tracks consumer complaints
about meat, poultry, and egg products.
Consumer complaints are usually filed
when food makes a consumer sick,
causes an allergic reaction, is not
properly labeled (misbranded), or
contains a foreign object. FSIS uses a
web portal to allow consumers to
electronically file a complaint with the
Agency about a meat, poultry, or egg
product. FSIS uses this information to
look for trends that will enhance the
Agency’s food safety efforts.
FSIS has made the following
estimates based upon an information
collection assessment.
Estimate of Burden: The public
reporting burden for this collection of
information is estimated to average 15
minutes per response.
Respondents: Consumers and
organizations.
Estimated Number of Respondents:
The CCMS web portal will have
approximately 3,000 respondents.
Estimated Number of Responses per
Respondent: 1.
Estimated Total Annual Burden on
Respondents: The total annual burden
time is estimated to be about 750 hours
for respondents using the CCMS web
portal.
All responses to this notice will be
summarized and included in the request
for OMB approval. All comments will
also become a matter of public record.
Copies of this information collection
assessment can be obtained from Gina
Kouba, Office of Policy and Program
Development, Food Safety and
Inspection Service, USDA, 1400
Independence Avenue SW, Mailstop
3758, South Building, Washington, DC
20250–3700; (202) 720–5627.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of FSIS’s functions, including whether
the information will have practical
utility; (b) the accuracy of FSIS’s
estimate of the burden of the proposed
collection of information, including the
validity of the method and assumptions
used; (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, including through the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques, or other forms of
information technology. Comments may
be sent to both FSIS, at the addresses
provided above, and the Desk Officer for
Agriculture, Office of Information and
Regulatory Affairs, Office of
Management and Budget (OMB),
Washington, DC 20253.
Responses to this notice will be
summarized and included in the request
for OMB approval. All comments will
also become a matter of public record.
Additional Public Notification
Public awareness of all segments of
rulemaking and policy development is
important. Consequently, FSIS will
announce this Federal Register
publication on-line through the FSIS
web page located at: http://
www.fsis.usda.gov/federal-register.
FSIS will also announce and provide
a link to this Federal Register
publication through the FSIS
Constituent Update, which is used to
provide information regarding FSIS
policies, procedures, regulations,
Federal Register notices, FSIS public
meetings, and other types of information
that could affect or would be of interest
to our constituents and stakeholders.
The Constituent Update is available on
the FSIS web page. Through the web
page, FSIS can provide information to a
much broader, more diverse audience.
In addition, FSIS offers an email
subscription service which provides
automatic and customized access to
selected food safety news and
information. This service is available at:
http://www.fsis.usda.gov/subscribe.
Options range from recalls to export
information, regulations, directives, and
notices. Customers can add or delete
subscriptions themselves and have the
option to password protect their
accounts.
USDA Non-Discrimination Statement
No agency, officer, or employee of the
USDA shall, on the grounds of race,
color, national origin, religion, sex,
gender identity, sexual orientation,
disability, age, marital status, family/
parental status, income derived from a
public assistance program, or political
beliefs, exclude from participation in,
deny the benefits of, or subject to
discrimination any person in the United
States under any program or activity
conducted by the USDA.
How to File a Complaint of
Discrimination
To file a complaint of discrimination,
complete the USDA Program
Discrimination Complaint Form, which
may be accessed online at http://
www.ocio.usda.gov/sites/default/files/
docs/2012/Complain_combined_6_8_
12.pdf, or write a letter signed by you
or your authorized representative.
Send your completed complaint form
or letter to USDA by mail, fax, or email:
Mail: U.S. Department of Agriculture,
Director, Office of Adjudication, 1400
Independence Avenue SW, Washington,
DC 20250–9410.
Fax: (202) 690–7442
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Email: program.intake@usda.gov
Persons with disabilities who require
alternative means for communication
(Braille, large print, audiotape, etc.),
should contact USDA’s TARGET Center
at (202) 720–2600 (voice and TDD).
Theresa Nintemann,
Acting Administrator.
[FR Doc. 2021–05734 Filed 3–18–21; 8:45 am]
BILLING CODE 3410–DM–P
DEPARTMENT OF COMMERCE
Economic Development Administration
Notice of Petitions by Firms for
Determination of Eligibility To Apply
for Trade Adjustment Assistance
AGENCY
: Economic Development
Administration, U.S. Department of
Commerce.
ACTION
: Notice and opportunity for
public comment.
SUMMARY
: The Economic Development
Administration (EDA) has received
petitions for certification of eligibility to
apply for Trade Adjustment Assistance
from the firms listed below.
Accordingly, EDA has initiated
investigations to determine whether
increased imports into the United States
of articles like or directly competitive
with those produced by each of the
firms contributed importantly to the
total or partial separation of the firms’
workers, or threat thereof, and to a
decrease in sales or production of each
petitioning firm.
SUPPLEMENTARY INFORMATION
:
L
IST OF
P
ETITIONS
R
ECEIVED BY
EDA
FOR
C
ERTIFICATION OF
E
LIGIBILITY
T
O
A
PPLY FOR
T
RADE
A
DJUSTMENT
A
SSISTANCE
[3/9/2021 through 3/12/2021]
Firm name Firm address Date
accepted for
investigation Product(s)
WireCo WorldGroup, Inc ......................... 2400 West 75th Street, Prairie Village,
KS 66208. 3/10/2021 The firm manufactures steel wire and
steel rope.
Walker Tool & Die, Inc ............................ 2411 Walker Avenue Northwest, Grand
Rapids, MI 49544. 3/10/2021 The firm manufactures metal stamping
dies.
Kenney Industries, Inc ............................. 2110 Panoramic Circle, Dallas, TX
75212. 3/11/2021 The firm manufactures miscellaneous
metal parts.
R & J Metal Finishing, Inc ....................... 273 Gould Avenue, Depew, NY 14043 ... 3/11/2021 The firm provides metal plating and
metal coating services.
Reel Power Industrial, Inc ....................... 5101 South Council Road, Oklahoma
City, OK 73179. 3/12/2021 The firm manufactures machinery for
reeling and coiling.
Any party having a substantial
interest in these proceedings may
request a public hearing on the matter.
A written request for a hearing must be
submitted to the Trade Adjustment
Assistance Division, Room 71030,
Economic Development Administration,
U.S. Department of Commerce,
Washington, DC 20230, no later than ten
(10) calendar days following publication
of this notice. These petitions are
received pursuant to section 251 of the
Trade Act of 1974, as amended.
Please follow the requirements set
forth in EDA’s regulations at 13 CFR
315.9 for procedures to request a public
hearing. The Catalog of Federal
Domestic Assistance official number
and title for the program under which
these petitions are submitted is 11.313,
Trade Adjustment Assistance for Firms.
Bryan Borlik,
Director.
[FR Doc. 2021–05656 Filed 3–18–21; 8:45 am]
BILLING CODE 3510–WH–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–21–2021]
Foreign-Trade Zone (FTZ) 99—
Wilmington, Delaware; Notification of
Proposed Production Activity;
AstraZeneca Pharmaceuticals LP
(Pharmaceutical Products); Newark,
Delaware
AstraZeneca Pharmaceuticals LP
(AstraZeneca) submitted a notification
of proposed production activity to the
FTZ Board for its facility in Newark,
Delaware. The notification conforming
to the requirements of the regulations of
the FTZ Board (15 CFR 400.22) was
received on March 11, 2021.
AstraZeneca already has authority to
produce certain pharmaceutical
products within Subzone 99D. The
current request would add finished
products and foreign status materials to
the scope of authority. Pursuant to 15
CFR 400.14(b), additional FTZ authority
would be limited to the specific foreign-
status materials and specific finished
products described in the submitted
notification (as described below) and
subsequently authorized by the FTZ
Board.
Production under FTZ procedures
could exempt AstraZeneca from
customs duty payments on the foreign-
status materials/components used in
export production. On its domestic
sales, for the foreign-status materials/
components noted below and in the
existing scope of authority, AstraZeneca
would be able to choose the duty rates
during customs entry procedures that
apply to: CALQUENCE (acalabrutinib)
capsules; DAKLINZA (daclatasvir)
tablets; FARXIGA\FORXIGA
(dapagliflozin) tablets; KOMBIGLYZE IR
(metformin hydrochloride and
saxagliptin hydrochloride) tablets;
KOMBIGLYZE XR (metformin
hydrochloride and saxagliptin
hydrochloride) tablets; METFORMIN IR
(metformin hydrochloride) tablets;
ONGLYZA (saxagliptin hydrochloride)
tablets; QTERN (dapagliflozin and
saxagliptin hydrochloride) tablets;
QTERNMET XR (dapagliflozin,
metformin hydrochloride and
saxagliptin hydrochloride) tablets;
TAGRISSO (osimertinib mesylate)
tablets; XIGDUO IR (dapagliflozin and
metformin hydrochloride) tablets;
XIGDUO XR (dapagliflozin & metformin
hydrochloride) tablets; and, CRESTOR
(rosuvastatin calcium) tablets (duty-
free). AstraZeneca would be able to
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