General Administrative Regulations; Administrative Remedies for Non-Compliance; Correcting Amendments, 11643 [E9-5793]
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Federal Register / Vol. 74, No. 52 / Thursday, March 19, 2009 / Rules and Regulations
11643
Dated: March 11, 2009.
Carol Waller Pope,
Acting Chairman.
[FR Doc. E9–5694 Filed 3–18–09; 8:45 am]
comply with a requirement of FCIC. The
term ‘‘requirement of this title’’ is
confusing and provides no reference to
a specific requirement.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 6727–01–P
List of Subjects in 7 CFR Parts 407 and
457
21 CFR Part 522
DEPARTMENT OF AGRICULTURE
Federal Crop Insurance Corporation
Administrative practice and
procedures; Administrative remedies for
non-compliance.
Implantation or Injectable Dosage
Form New Animal Drugs; Tylosin
7 CFR Parts 400, 407, 457
■
RIN 0563–AB73
General Administrative Regulations;
Administrative Remedies for NonCompliance; Correcting Amendments
AGENCY: Federal Crop Insurance
Corporation, USDA.
ACTION: Final rule; correcting
amendment.
2. In § 407.9 amend item 22 by
revising paragraph (a)(1) to read as
follows:
■
This document contains
correcting amendments to the final
regulations that were published
December 18, 2008 (73 FR 76868–
76891). These regulations pertain to
Administrative Remedies for NonCompliance and provide clarification of
existing remedies.
DATES: Effective Date: March 19, 2009.
FOR FURTHER INFORMATION CONTACT:
Cynthia Simpson, Director, Appeals,
Litigation and Legal Liaison Staff, Risk
Management Agency, United States
Department of Agriculture, 1400
Independence Avenue, SW., Room
6603, Stop 0806, Washington, DC
20250, telephone (202) 720–0642.
SUPPLEMENTARY INFORMATION:
§ 407.9
Group risk plan common policy.
*
*
*
*
*
22. Remedial Sanctions
*
*
*
*
*
(a) * * *
(1) The amount of the pecuniary gain
obtained as a result of the false or
inaccurate information provided or the
noncompliance with a requirement of
FCIC; or
*
*
*
*
*
PART 457—COMMON CROP
INSURANCE REGULATIONS
3. In § 457.8 amend item 27 by
revising paragraph (e)(1)(i) to read as
follows:
■
Background
The final regulation that is the subject
of these correcting amendments was
intended to add additional
administrative remedies that are
available as a result of the enactment of
section 515(h) of the Federal Crop
Insurance Act (Act) (7 U.S.C. 1515(h)),
make such other changes as are
necessary to implement the provisions
of section 515(h) of the Act, and to
clarify existing administrative remedies.
Need for Corrections
mstockstill on PROD1PC66 with RULES
Authority: 7 U.S.C. 1506(l) and 1506(o).
PART 407—GROUP RISK PLAN OF
INSURANCE REGULATIONS
SUMMARY:
As published, the final regulation
contained an error that may prove to be
misleading and needs to be clarified.
On page 73 FR 76891 in § 407.9 item
22(a)(1) and § 457.8 item 27(e)(1)(i) the
term ‘‘requirement of this title’’ is
incorrect and should read ‘‘requirement
of FCIC.’’ Section 515(h) of the Act
authorizes disqualification and the
assessment of civil fine of persons who
willfully and intentionally provide false
or inaccurate information or fails to
VerDate Nov<24>2008
Accordingly, the 7 CFR part 407 and
457 is amended as follows:
■ 1. The authority citation for 7 CFR
part 407 and 457 is revised to read as
follows:
18:17 Mar 18, 2009
Jkt 217001
§ 457.8
The application and policy.
*
*
*
*
*
27. Concealment, Misrepresentation
or Fraud.
*
*
*
*
*
(e) * * *
(1) * * *
(i) The amount of the pecuniary gain
obtained as a result of the false or
inaccurate information provided or the
noncompliance with a requirement of
FCIC; or
*
*
*
*
*
Signed in Washington, DC, on March 11,
2009.
William J. Murphy,
Acting Manager, Federal Crop Insurance
Corporation.
[FR Doc. E9–5793 Filed 3–18–09; 8:45 am]
BILLING CODE 3410–08–P
PO 00000
Frm 00005
Fmt 4700
Sfmt 4700
Food and Drug Administration
[Docket No. FDA–2009–N–0665]
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final rule.
SUMMARY: The Food and Drug
Administration (FDA) is amending the
animal drug regulations to reflect
approval of a supplemental new animal
drug application (NADA) filed by
Elanco Animal Health. The
supplemental NADA provides for
changing scientific nomenclature for a
bovine pathogen on labeling for tylosin
injectable solution.
DATES: This rule is effective March 19,
2009.
FOR FURTHER INFORMATION CONTACT:
Cindy L. Burnsteel, Center for
Veterinary Medicine (HFV–130), Food
and Drug Administration, 7500 Standish
Pl., Rockville, MD 20855, 240–276–
8341, e-mail:
cindy.burnsteel@fda.hhs.gov.
Elanco
Animal Health, A Division of Eli Lilly
& Co., Lilly Corporate Center,
Indianapolis, IN 46285, filed a
supplement to NADA 12–965 for
TYLAN (tylosin) Injection, an injectable
solution used for the treatment of
animal diseases associated with several
bacterial pathogens. The supplemental
NADA provides for changing a bovine
pathogen name on product labeling. The
supplemental NADA is approved as of
February 24, 2009, and the regulations
in 21 CFR 522.2640 and 522.2640a are
amended to reflect the approval.
Approval of this supplemental NADA
did not require review of additional
safety or effectiveness data or
information. Therefore, a freedom of
information summary is not required.
The agency has determined under 21
CFR 25.33(a)(1) that this action is of a
type that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
nor an environmental impact statement
is required.
This rule does not meet the definition
of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because
it is a rule of ‘‘particular applicability.’’
Therefore, it is not subject to the
congressional review requirements in 5
U.S.C. 801–808.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\19MRR1.SGM
19MRR1
]]>Agencies
[Federal Register Volume 74, Number 52 (Thursday, March 19, 2009)]
[Rules and Regulations]
[Page 11643]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-5793]
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DEPARTMENT OF AGRICULTURE
Federal Crop Insurance Corporation
7 CFR Parts 400, 407, 457
RIN 0563-AB73
General Administrative Regulations; Administrative Remedies for
Non-Compliance; Correcting Amendments
AGENCY: Federal Crop Insurance Corporation, USDA.
ACTION: Final rule; correcting amendment.
-----------------------------------------------------------------------
SUMMARY: This document contains correcting amendments to the final
regulations that were published December 18, 2008 (73 FR 76868-76891).
These regulations pertain to Administrative Remedies for Non-Compliance
and provide clarification of existing remedies.
DATES: Effective Date: March 19, 2009.
FOR FURTHER INFORMATION CONTACT: Cynthia Simpson, Director, Appeals,
Litigation and Legal Liaison Staff, Risk Management Agency, United
States Department of Agriculture, 1400 Independence Avenue, SW., Room
6603, Stop 0806, Washington, DC 20250, telephone (202) 720-0642.
SUPPLEMENTARY INFORMATION:
Background
The final regulation that is the subject of these correcting
amendments was intended to add additional administrative remedies that
are available as a result of the enactment of section 515(h) of the
Federal Crop Insurance Act (Act) (7 U.S.C. 1515(h)), make such other
changes as are necessary to implement the provisions of section 515(h)
of the Act, and to clarify existing administrative remedies.
Need for Corrections
As published, the final regulation contained an error that may
prove to be misleading and needs to be clarified.
On page 73 FR 76891 in Sec. 407.9 item 22(a)(1) and Sec. 457.8
item 27(e)(1)(i) the term ``requirement of this title'' is incorrect
and should read ``requirement of FCIC.'' Section 515(h) of the Act
authorizes disqualification and the assessment of civil fine of persons
who willfully and intentionally provide false or inaccurate information
or fails to comply with a requirement of FCIC. The term ``requirement
of this title'' is confusing and provides no reference to a specific
requirement.
List of Subjects in 7 CFR Parts 407 and 457
Administrative practice and procedures; Administrative remedies for
non-compliance.
0
Accordingly, the 7 CFR part 407 and 457 is amended as follows:
0
1. The authority citation for 7 CFR part 407 and 457 is revised to read
as follows:
Authority: 7 U.S.C. 1506(l) and 1506(o).
PART 407--GROUP RISK PLAN OF INSURANCE REGULATIONS
0
2. In Sec. 407.9 amend item 22 by revising paragraph (a)(1) to read as
follows:
Sec. 407.9 Group risk plan common policy.
* * * * *
22. Remedial Sanctions
* * * * *
(a) * * *
(1) The amount of the pecuniary gain obtained as a result of the
false or inaccurate information provided or the noncompliance with a
requirement of FCIC; or
* * * * *
PART 457--COMMON CROP INSURANCE REGULATIONS
0
3. In Sec. 457.8 amend item 27 by revising paragraph (e)(1)(i) to read
as follows:
Sec. 457.8 The application and policy.
* * * * *
27. Concealment, Misrepresentation or Fraud.
* * * * *
(e) * * *
(1) * * *
(i) The amount of the pecuniary gain obtained as a result of the
false or inaccurate information provided or the noncompliance with a
requirement of FCIC; or
* * * * *
Signed in Washington, DC, on March 11, 2009.
William J. Murphy,
Acting Manager, Federal Crop Insurance Corporation.
[FR Doc. E9-5793 Filed 3-18-09; 8:45 am]
BILLING CODE 3410-08-P
