Facility License; Correction

CourtNational Indian Gaming Commission
Citation87 FR 2095
Record Number2022-00625
Publication Date13 January 2022
2095
Federal Register / Vol. 87, No. 9 / Thursday, January 13, 2022 / Proposed Rules
IV. Participating in the Public Hearing
Registration: To register to attend the
virtual public hearing, on ‘‘Scientific
Data and Information Related to the
Residue of Carcinogenic Concern for the
New Animal Drug Carbadox; Public
Hearing; Request for Comments’’ please
register at https://fda.zoomgov.com/j/
1600135012?
pwd=MFdjMW9FRXg4RGllc
3FHWVhkWVAyZz09 by March 9, 2022.
If you have any questions, you can
contact CarbadoxPublicHearing2022@
fda.hhs.gov (See
DATES
and
ADDRESSES
).
Please provide complete contact
information for each attendee, including
name, title, affiliation, address, email,
and telephone.
Request for Oral Presentations: During
online registration, you may indicate if
you wish to make a formal presentation
(with accompanying slide deck) or
present oral comments during the
public hearing session (with no slide
deck). If you decide you wish to make
a presentation after registering online,
you may submit a request to
CarbadoxPublicHearing2022@
fda.hhs.gov. All requests to make
presentations must be received by
February 18, 2022. FDA will do its best
to accommodate requests to make public
presentations. Individuals and
organizations with common interests are
urged to consolidate or coordinate their
presentations. FDA will determine the
amount of time allotted to each
presenter and the approximate time
each presentation is to begin and will
select and notify participants by
February 23, 2022.
If selected for a formal oral
presentation (with a slide deck), each
presenter must submit an electronic
copy of their presentation (PowerPoint
or PDF) to
CarbadoxPublicHearing2022@
fda.hhs.gov with the subject line
‘‘Scientific Data and Information
Related to the Residue of Carcinogenic
Concern for the New Animal Drug
Carbadox; Public Hearing; Request for
Comments’’ on or before March 4, 2022.
No commercial or promotional material
will be permitted to be presented or
distributed at the public hearing.
Persons notified that they will be
presenters are encouraged to be online
early. Actual presentation times may
vary based on how the hearing
progresses in real time. An agenda for
the hearing and any other background
materials will be made available no later
than 5 days before the hearing at https://
www.fda.gov/animal-veterinary/
workshops-conferences-meetings/part-
15-public-hearing-scientific-data-and-
information-related-residue-
carcinogenic-concern-new.
Transcripts: Please be advised that as
soon as a transcript of the public
hearing is available, it will be accessible
at https://www.regulations.gov. It may
also be viewed at the Dockets
Management Staff (see
ADDRESSES
). A
link to the transcript will also be
available on the Agency’s website at
https://www.fda.gov/animal-veterinary/
workshops-conferences-meetings/part-
15-public-hearing-scientific-data-and-
information-related-residue-
carcinogenic-concern-new.
Dated: January 7, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022–00475 Filed 1–12–22; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF THE INTERIOR
National Indian Gaming Commission
25 CFR Part 559
RIN 3141–AA76
Facility License; Correction
AGENCY
: National Indian Gaming
Commission, Department of the Interior.
ACTION
: Proposed rule; correction.
SUMMARY
: This document corrects the
preamble to a proposed rule published
in the Federal Register of December 1,
2021, regarding Facility Licenses. The
document contained incorrect dates for
submitting comments. This correction
clarifies that comments are due January
31, 2022.
FOR FURTHER INFORMATION CONTACT
:
Michael Hoenig, 202–632–7003.
SUPPLEMENTARY INFORMATION
:
Correction
In the Federal Register of December 1,
2021, in FR Doc. 2021–25845, on page
68200, in the third column, change the
DATES
caption to read:
DATES
: Written comments on this
proposed rule must be received on or
before January 31, 2022.
Dated: January 6, 2022.
Michael Hoenig,
General Counsel.
[FR Doc. 2022–00625 Filed 1–12–22; 8:45 am]
BILLING CODE 7565–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R04–OAR–2021–0428; FRL–9374–01–
R4]
Finding of Failure To Attain the 2010
Sulfur Dioxide Standard; Tennessee;
Sullivan County Nonattainment Area
AGENCY
: Environmental Protection
Agency (EPA).
ACTION
: Proposed rule.
SUMMARY
: The Environmental Protection
Agency (EPA) is proposing to determine
that the Sullivan County, Tennessee
sulfur dioxide (SO
2
) nonattainment area
failed to attain the 2010 1-hour SO
2
primary National Ambient Air Quality
Standard (NAAQS or standard) by the
applicable attainment date of October 4,
2018, based upon a weight of evidence
analysis of available quality-assured and
certified SO
2
ambient air monitoring
data and SO
2
emissions data from
January 2015 through December 2017. If
EPA finalizes this determination as
proposed, the State of Tennessee will be
required to submit revisions to the
Tennessee State Implementation Plan
(SIP) that, among other elements,
provide for expeditious attainment of
the 2010 SO
2
standard.
DATES
: Comments must be received on
or before February 14, 2022.
ADDRESSES
: Submit your comments,
identified by Docket ID No. EPA–R04–
OAR–2021–0428 at https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Once submitted, comments cannot be
edited or removed from Regulations.gov.
EPA may publish any comment received
to its public docket. Do not submit
electronically any information you
consider to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Multimedia submissions (audio, video,
etc.) must be accompanied by a written
comment. The written comment is
considered the official comment and
should include discussion of all points
you wish to make. EPA will generally
not consider comments or comment
contents located outside of the primary
submission (i.e., on the web, cloud, or
other file sharing system). For
additional submission methods, the full
EPA public comment policy,
information about CBI or multimedia
submissions, and general guidance on
making effective comments, please visit
https://www2.epa.gov/dockets/
commenting-epa-dockets.
FOR FURTHER INFORMATION CONTACT
:
Evan Adams, Air Regulatory
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