Proposed Data Collection Submitted for Public Comment and Recommendations, 54000-54002 [2024-14309]
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khammond on DSKJM1Z7X2PROD with NOTICES
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Federal Register / Vol. 89, No. 125 / Friday, June 28, 2024 / Notices
of Purpose for an Extension of Credit by
a Creditor (FR T–4), and Statement of
Purpose for an Extension of Credit
Secured by Margin Stock (FR U–1).
These reports relate to extensions of
credit secured by margin stock. The
Board collects the information gathered
by the Margin Credit Reports so that it
may meet certain obligations under the
Securities Exchange Act of 1934.
Certain lenders that are not brokers,
dealers, or banks making loans secured
by margin stock must register and
deregister with the Federal Reserve
using the FR G–1 and FR G–2,
respectively, and must file an annual
report (FR G–4) while registered. The FR
G–1, FR G–2, and FR G–4 reporting
requirements collect data used to
identify lenders subject to the Board’s
Regulation U to verify their compliance
with the regulation and to monitor
margin credit.
The FR T–4, FR U–1, and FR G–3 are
forms that implement recordkeeping
requirements for brokers and dealers,
banks, and other lenders, respectively.
The FR T–4 documents the purpose of
credit being extended when that credit
is not to purchase, carry, or trade in
securities and the credit is in excess of
that otherwise permitted under
Regulation T. The FR G–3 and FR U–1
document the purpose of loans secured
by margin stock.
Frequency: The FR G–1, FR G–2, FR
G–3, FR T–4, and FR U–1 are eventgenerated; the FR G–4 is completed
annually.
Respondents: The FR G–1, FR G–2, FR
G–3, and FR G–4 panels comprise
lenders, other than banks, brokers, or
dealers, that extend margin credit,
including federal and state credit
unions; insurance companies;
commercial and consumer credit
organizations; production credit
associations; small businesses;
insurance premium funding plans; planlenders (a company or its affiliate that
extends credit to employees to purchase
company stock under an eligible
employee stock option or stock
purchase plan); and lenders to
Employee Stock Ownership Plans
(ESOPs), thrift plans, and broker-dealer
affiliates. The FR T–4 panel comprises
brokers and dealers and the FR U–1
panel comprises banks.
Total estimated number of
respondents: FR G–1, 25; FR G–2, 12; FR
G–3, 10; FR G–4, 129; FR T–4, 14; FR
U–1, 14.
Estimated average hours per response:
FR G–1, 1.65; FR G–2, 0.53; FR G–3,
0.25; FR G–4, 2.07; FR T–4, 0.25; FR U–
1, 0.25.
Total estimated annual burden hours:
697.
VerDate Sep<11>2014
19:25 Jun 27, 2024
Jkt 262001
Current actions: On February 16,
2024, the Board published a notice in
the Federal Register (89 FR 12342)
requesting public comment for 60 days
on the extension, with revision, of the
FR G–1, FR G–2, FR G–3, FR G–4, FR
T–4, and FR U–1. The Board revised the
FR G–1 and FR G–4 by updating the
confidentiality treatment as contained
in the reporting instructions to state that
individual respondents may request that
information submitted to the Board
through the FR G–1 and FR G–4 be kept
confidential and the Board will evaluate
whether such treatment is appropriate
on a case-by-case basis. The comment
period for this notice expired on April
16, 2024. The Board did not receive any
comments.
Board of Governors of the Federal Reserve
System, June 25, 2024.
Benjamin W. McDonough,
Deputy Secretary and Ombuds of the Board.
[FR Doc. 2024–14341 Filed 6–27–24; 8:45 am]
BILLING CODE 6210–01–P
GENERAL SERVICES
ADMINISTRATION
[Notice–MEG–2024–02; Docket No. 2024–
0002; Sequence No. 29]
Notice of Establishment of a Federal
Advisory Committee
Office of Government-wide
Policy, General Services Administration
(GSA).
ACTION: Notice.
AGENCY:
The General Services
Administration (GSA) announces the
establishment of the Open Government
Federal Advisory Committee
(hereinafter ‘‘the Committee’’ or ‘‘the
OG FAC’’) in accordance with the
Federal Advisory Committee Act, as
amended.
DATES: June 28, 2024.
FOR FURTHER INFORMATION CONTACT:
Arthur Brunson, Designated Federal
Officer, Office of Government-wide
Policy, 202–501–1126, or email:
arthur.brunson@gsa.gov; or email:
ogfac@gsa.gov.
SUPPLEMENTARY INFORMATION: The
Administrator of the U.S. General
Services Administration (GSA)
established the Open Government
Federal Advisory Committee (OG FAC)
as a discretionary advisory committee
under agency authority in accordance
with the provisions of the Federal
Advisory Committee Act (FACA), as
amended, 5 U.S.C. 10. GSA has
determined that the establishment of OG
FAC is necessary and in the public
interest.
SUMMARY:
PO 00000
Frm 00063
Fmt 4703
Sfmt 4703
GSA’s Open Government Secretariat
supports ensuring a more transparent,
responsive and inclusive Federal
Government. This is done by providing
channels for members of the public to
regularly engage with their government.
The OG FAC will advise GSA in its
endeavor to increase the public’s access
to data, to better advance equity, engage
the public in the regulatory process,
make government records more
accessible, and improve the delivery of
government services and benefits
through expert advice.
The OG FAC will serve as an advisory
body to GSA on GSA Open Government
initiatives including GSA’s creation,
implementation and monitoring of U.S.
Open Government National Action
Plans (NAPs) and commitment themes.
The initial focus for the OG FAC will be
to provide advice to GSA on the
development of NAP 6, Open
Government Policy, and Public
Engagement. The OG FAC will advise
GSA’s Administrator on emerging open
government issues, challenges and
opportunities to support GSA’s Open
Government Secretariat.
The OG FAC advisory committee is
essential to conduct agency business for
GSA and bring together civil society,
Federal agencies, academia, industry,
and other interested stakeholders. GSA
needs a wide diversity of views on Open
Government initiatives.
Mehul Parekh,
Acting Associate Administrator, Office of
Government-wide Policy, General Services
Administration.
[FR Doc. 2024–14259 Filed 6–27–24; 8:45 am]
BILLING CODE 6820–UA–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24GU; Docket No. CDC–2024–
0053]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other federal
agencies the opportunity to comment on
SUMMARY:
E:\FR\FM\28JNN1.SGM
28JNN1
54001
Federal Register / Vol. 89, No. 125 / Friday, June 28, 2024 / Notices
a proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Assessing
Adoption and Implementation of the
National Institute of Occupational
Safety and Health’s (NIOSH) Outputs.
NIOSH proposes using surveys,
interviews, and focus groups to improve
awareness, understanding, and assess
the impact of adoption and
implementation practices by users of
NIOSH research efforts and products.
DATES: CDC must receive written
comments on or before August 27, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0053 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires federal agencies to provide a
60-day notice in the Federal Register
With the continuation of the
Government Performance and Results
Act, and the more recent passage of the
Foundations of Evidence-Based Policy
Making Act, there is an increased need
for federal agencies to measure and
demonstrate their impact. However,
measuring impact is challenging,
especially for organizations that have a
science-driven mission because of the
time it takes to move from basic to
applied research. Demonstrating
attribution (cause and effect
relationships) is particularly challenging
for research organizations. NIOSH
research is often designed to collect
implementation and adoption data
through document reviews of NIOSH
records, including grantee final reports,
and through interviews with NIOSH
researchers (federal employees). While
commonly recognized metrics, these
data sources are not comprehensive,
representative, or informative of the
adoption and implementation of NIOSH
products and efforts. Further, the design
and execution of research projects has
hindered research and program leaders
prioritizing information collections to
understand and assess the adoption and
implementation of research efforts and
products.
The proposed Generic information
collection package would allow
researchers to expeditiously pursue
efforts to provide NIOSH with critical
information to inform mission-driven
needs. Additionally, the proposed
efforts go beyond simply measuring
customer satisfaction and seek to
advance NIOSH’s burden, need, and
impact framework for future research
while also endeavoring to execute the
Office of Management and Budget’s
guidance regarding the Foundations of
Evidence-Based Policymaking Act.
Respondents are expected to consist of
users and potential users of NIOSH
products including subject matter
expects, former NIOSH funding
recipients, and intermediary and end
users. CDC requests OMB approval for
an estimated 6,069 annual burden
hours. There is no cost to respondents
other than their time to participate.
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Assessing Adoption and
Implementation of the National Institute
of Occupational Safety and Health’s
(NIOSH) Outputs—New—National
Institute of Occupational Safety and
Health’s (NIOSH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), National Institute for
Occupational Safety and Health
(NIOSH), is requesting approval of a
new Generic information collection for
a period of three years for the project
titled, Assessing Adoption and
Implementation of the National Institute
of Occupational Safety and Health’s
(NIOSH) Outputs.
khammond on DSKJM1Z7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Type of data collection instrument
Subject matter experts ......................
Survey instrument (pre and post) ....
Informed consent form .....................
Interview or focus group guide ........
Survey instrument (pre and post) ....
Informed consent form .....................
Former NIOSH funding recipients ....
VerDate Sep<11>2014
19:25 Jun 27, 2024
Jkt 262001
PO 00000
Frm 00064
Fmt 4703
Number of
respondents
Sfmt 4703
Number of
responses per
respondent
5,000
250
250
200
25
E:\FR\FM\28JNN1.SGM
1
1
1
1
1
28JNN1
Average
burden per
response
(in hours)
20/60
5/60
1
20/60
5/60
Total burden
hours
1,667
21
250
67
2
54002
Federal Register / Vol. 89, No. 125 / Friday, June 28, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of respondent
Type of data collection instrument
Intermediary or end users (e.g., employers, workers, manufactures,
labor/professional
associations,
policymakers).
Total ...........................................
1
1
1
1
20/60
5/60
25
3,333
54
Interview or focus group guide ........
650
1
1
650
...........................................................
........................
........................
........................
6,069
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
[FR Doc. 2024–14289 Filed 6–27–24; 8:45 am]
Advisory Committee on Breast Cancer
in Young Women; Notice of Charter
Renewal
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of charter renewal.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), within
the Department of Health and Human
Services (HHS), announces the renewal
of the charter of the Advisory
Committee on Breast Cancer in Young
Women (ACBCYW).
FOR FURTHER INFORMATION CONTACT:
Kimberly E. Smith, M.B.A., M.H.A.,
Designated Federal Officer, Advisory
Committee on Breast Cancer in Young
Women, Centers for Disease Control and
Prevention, Department of Health and
Human Services, 4770 Buford Highway
NE, Mailstop S107–4, Atlanta, Georgia
30341–3717. Telephone: (404) 498–
0073; Email: KESmith@cdc.gov.
SUPPLEMENTARY INFORMATION: CDC is
providing notice under 5 U.S.C. 1001–
1014 of the renewal of the charter of the
Advisory Committee on Breast Cancer
in Young Women, Centers for Disease
Control and Prevention, Department of
Health and Human Services. This
charter has been renewed for a two-year
period through June 17, 2026.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
SUMMARY:
Jkt 262001
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
khammond on DSKJM1Z7X2PROD with NOTICES
Total burden
hours
25
10,000
650
[FR Doc. 2024–14309 Filed 6–27–24; 8:45 am]
19:25 Jun 27, 2024
Average
burden per
response
(in hours)
Interview or focus group guide ........
Survey instrument (pre and post) ....
Informed consent form .....................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
VerDate Sep<11>2014
Number of
responses per
respondent
Number of
respondents
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–179, CMS–
10536, CMS–R–153 and CMS–10326]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
SUMMARY:
PO 00000
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Fmt 4703
Sfmt 4703
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
August 27, 2024.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number: Room C4–26–05, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
E:\FR\FM\28JNN1.SGM
28JNN1
]]>Agencies
[Federal Register Volume 89, Number 125 (Friday, June 28, 2024)]
[Notices]
[Pages 54000-54002]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-14309]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-24GU; Docket No. CDC-2024-0053]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
federal agencies the opportunity to comment on
[[Page 54001]]
a proposed information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Assessing Adoption and
Implementation of the National Institute of Occupational Safety and
Health's (NIOSH) Outputs. NIOSH proposes using surveys, interviews, and
focus groups to improve awareness, understanding, and assess the impact
of adoption and implementation practices by users of NIOSH research
efforts and products.
DATES: CDC must receive written comments on or before August 27, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0053 by either of the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to www.regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (www.regulations.gov) or by U.S. mail to the address listed
above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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, e.g., permitting electronic
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Assessing Adoption and Implementation of the National Institute of
Occupational Safety and Health's (NIOSH) Outputs--New--National
Institute of Occupational Safety and Health's (NIOSH), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), National
Institute for Occupational Safety and Health (NIOSH), is requesting
approval of a new Generic information collection for a period of three
years for the project titled, Assessing Adoption and Implementation of
the National Institute of Occupational Safety and Health's (NIOSH)
Outputs.
With the continuation of the Government Performance and Results
Act, and the more recent passage of the Foundations of Evidence-Based
Policy Making Act, there is an increased need for federal agencies to
measure and demonstrate their impact. However, measuring impact is
challenging, especially for organizations that have a science-driven
mission because of the time it takes to move from basic to applied
research. Demonstrating attribution (cause and effect relationships) is
particularly challenging for research organizations. NIOSH research is
often designed to collect implementation and adoption data through
document reviews of NIOSH records, including grantee final reports, and
through interviews with NIOSH researchers (federal employees). While
commonly recognized metrics, these data sources are not comprehensive,
representative, or informative of the adoption and implementation of
NIOSH products and efforts. Further, the design and execution of
research projects has hindered research and program leaders
prioritizing information collections to understand and assess the
adoption and implementation of research efforts and products.
The proposed Generic information collection package would allow
researchers to expeditiously pursue efforts to provide NIOSH with
critical information to inform mission-driven needs. Additionally, the
proposed efforts go beyond simply measuring customer satisfaction and
seek to advance NIOSH's burden, need, and impact framework for future
research while also endeavoring to execute the Office of Management and
Budget's guidance regarding the Foundations of Evidence-Based
Policymaking Act. Respondents are expected to consist of users and
potential users of NIOSH products including subject matter expects,
former NIOSH funding recipients, and intermediary and end users. CDC
requests OMB approval for an estimated 6,069 annual burden hours. There
is no cost to respondents other than their time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Type of data Number of Average burden
Type of respondent collection Number of responses per per response Total burden
instrument respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
Subject matter experts........ Survey 5,000 1 20/60 1,667
instrument (pre
and post).
Informed consent 250 1 5/60 21
form.
Interview or 250 1 1 250
focus group
guide.
Former NIOSH funding Survey 200 1 20/60 67
recipients. instrument (pre
and post).
Informed consent 25 1 5/60 2
form.
[[Page 54002]]
Interview or 25 1 1 25
focus group
guide.
Intermediary or end users Survey 10,000 1 20/60 3,333
(e.g., employers, workers, instrument (pre 650 1 5/60 54
manufactures, labor/ and post).
professional associations, Informed consent
policymakers). form.
Interview or 650 1 1 650
focus group
guide.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 6,069
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health
Ethics and Regulations, Office of Science, Centers for Disease Control
and Prevention.
[FR Doc. 2024-14309 Filed 6-27-24; 8:45 am]
BILLING CODE 4163-18-P
