Prevention of Salmonella, 18751 [2010-8358]
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18751
Rules and Regulations
Federal Register
Vol. 75, No. 70
Tuesday, April 13, 2010
This section of the FEDERAL REGISTER
contains regulatory documents having general
applicability and legal effect, most of which
are keyed to and codified in the Code of
Federal Regulations, which is published under
50 titles pursuant to 44 U.S.C. 1510.
Procedure Act (5 U.S.C. 553). Notice
and public procedures are unnecessary
because FDA is merely updating
nonsubstantive content.
DEPARTMENT OF JUSTICE
List of Subjects in 21 CFR Part 118
RIN 1110–AA26
The Code of Federal Regulations is sold by
the Superintendent of Documents. Prices of
new books are listed in the first FEDERAL
REGISTER issue of each week.
Eggs and egg products, Incorporation
by reference, Recordkeeping
requirements, Safety.
FBI Criminal Justice Information
Services Division User Fees
Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs, 21 CFR part 118 is
amended as follows:
■
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
PART 118—PRODUCTION, STORAGE,
AND TRANSPORTATION OF SHELL
EGGS
21 CFR Part 118
[Docket No. FDA–2000–N–0190]
Prevention of Salmonella Enteritidis in
Shell Eggs During Production,
Storage, and Transportation; Change
of Registration Date, Address, and
Telephone Number; Technical
Amendment
AGENCY:
Food and Drug Administration,
HHS.
SUMMARY: The Food and Drug
Administration (FDA) is amending its
regulations to correct the date by which
producers must register their farm with
FDA, reflect a change in the address and
telephone number for requesting copies
of Form No. 3733, and reflect a change
in the address to which producers must
send their CD–ROM. This action is
editorial in nature and is intended to
improve the accuracy of the agency’s
regulations.
Effective on April 13, 2010.
John
Sheehan, Center for Food Safety and
Applied Nutrition (HFS–315), Food and
Drug Administration, 5100 Paint Branch
Pkwy., College Park, MD 20740, 301–
436–1488.
SUPPLEMENTARY INFORMATION: FDA is
amending its regulations in 21 CFR part
118 to correct the following information:
(1) The date by which egg producers
must register their farm with FDA, (2)
the address and telephone number for
requesting copies of Form 3733, and (3)
the address to which egg producers
must send their CD–ROM. Publication
of this document constitutes final action
on this change under the Administrative
wwoods2 on DSK1DXX6B1PROD with RULES_PART 1
FOR FURTHER INFORMATION CONTACT:
VerDate Nov<24>2008
14:59 Apr 12, 2010
Authority: 21 U.S.C. 321, 331–334, 342,
371, 381, 393; 42 U.S.C. 243, 264, 271.
2. In § 118.11, revise paragraphs (a),
(b)(2)(i), and (b)(3)(vi) to read as follows:
■
§ 118.11 Registration requirements for
shell egg producers covered by the
requirements of this part.
Final rule; technical
amendment.
ACTION:
DATES:
1. The authority citation for 21 CFR
part 118 continues to read as follows:
■
Jkt 220001
(a) Shell egg producers covered under
§ 118.1(a) are required to register their
farms with FDA within 30 days of
becoming an egg producer or, if already
an egg producer, by each farm’s
applicable compliance date.
(b) * * *
(2) * * *
(i) You must register using FDA Form
No. 3733. You may obtain a copy of this
form by writing to the U.S. Food and
Drug Administration, 5600 Fishers Lane
(HFS–681), Rockville, MD 20857, or by
requesting the form by phone at 1–800–
216–7331 or 301–575–0156.
*
*
*
*
*
(3) * * *
(vi) You must mail the CD–ROM to
the U.S. Food and Drug Administration,
5600 Fishers Lane (HFS–681), Rockville,
MD 20857.
*
*
*
*
*
Dated: April 7, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–8358 Filed 4–12–10; 8:45 am]
BILLING CODE 4160–01–S
PO 00000
Frm 00001
Fmt 4700
Sfmt 4700
28 CFR Part 20
[Docket No. FBI 114]
AGENCY: Federal Bureau of Investigation
(FBI), Justice.
ACTION: Final rule.
SUMMARY: This Final Rule sets out the
Director of the FBI’s authority to
establish and collect fees for providing
fingerprint-based and name-based
Criminal History Record Information
(CHRI) checks and other identification
services submitted by authorized users
for noncriminal justice purposes,
including employment and licensing.
The FBI may set such fees at a level to
include an amount to establish a fund
to defray expenses for the automation of
fingerprint identification and criminal
justice information services and
associated costs. It further provides that
future fee adjustments will be made by
notice published in the Federal
Register.
DATES: This final rule is effective May
13, 2010.
FOR FURTHER INFORMATION CONTACT: FBI
Criminal Justice Information Services
Division, 1000 Custer Hollow Road,
Module E–3, Clarksburg, West Virginia
26306, Attention: Christopher L.
Enourato.
SUPPLEMENTARY INFORMATION:
I. Background
On June 19, 2008, the FBI published
a Notice of Proposed Rulemaking
(NPRM) setting forth the FBI’s statutory
authority to establish and collect fees for
noncriminal justice fingerprint-based
and name-based CHRI checks and other
identification services performed by the
CJIS Division. See 73 FR 34905 (2008)
(to be codified at 28 CFR part 20).
The NPRM explained the
methodology used to calculate the FBI’s
revised fees, provided a proposed fee
schedule, and advised that the current
fees would be published concurrently
with this Final Rule as a Notice in the
Federal Register. This Final Rule
implements the FBI’s statutory fee
authority. All future fee adjustments
will be made by Notice published in the
Federal Register.
E:\FR\FM\13APR1.SGM
13APR1
]]>Agencies
[Federal Register Volume 75, Number 70 (Tuesday, April 13, 2010)]
[Rules and Regulations]
[Page 18751]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-8358]
========================================================================
Rules and Regulations
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains regulatory documents
having general applicability and legal effect, most of which are keyed
to and codified in the Code of Federal Regulations, which is published
under 50 titles pursuant to 44 U.S.C. 1510.
The Code of Federal Regulations is sold by the Superintendent of Documents.
Prices of new books are listed in the first FEDERAL REGISTER issue of each
week.
========================================================================
Federal Register / Vol. 75, No. 70 / Tuesday, April 13, 2010 / Rules
and Regulations
[[Page 18751]]
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 118
[Docket No. FDA-2000-N-0190]
Prevention of Salmonella Enteritidis in Shell Eggs During
Production, Storage, and Transportation; Change of Registration Date,
Address, and Telephone Number; Technical Amendment
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; technical amendment.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is amending its
regulations to correct the date by which producers must register their
farm with FDA, reflect a change in the address and telephone number for
requesting copies of Form No. 3733, and reflect a change in the address
to which producers must send their CD-ROM. This action is editorial in
nature and is intended to improve the accuracy of the agency's
regulations.
DATES: Effective on April 13, 2010.
FOR FURTHER INFORMATION CONTACT: John Sheehan, Center for Food Safety
and Applied Nutrition (HFS-315), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740, 301-436-1488.
SUPPLEMENTARY INFORMATION: FDA is amending its regulations in 21 CFR
part 118 to correct the following information: (1) The date by which
egg producers must register their farm with FDA, (2) the address and
telephone number for requesting copies of Form 3733, and (3) the
address to which egg producers must send their CD-ROM. Publication of
this document constitutes final action on this change under the
Administrative Procedure Act (5 U.S.C. 553). Notice and public
procedures are unnecessary because FDA is merely updating
nonsubstantive content.
List of Subjects in 21 CFR Part 118
Eggs and egg products, Incorporation by reference, Recordkeeping
requirements, Safety.
0
Therefore, under the Federal Food, Drug, and Cosmetic Act and under
authority delegated to the Commissioner of Food and Drugs, 21 CFR part
118 is amended as follows:
PART 118--PRODUCTION, STORAGE, AND TRANSPORTATION OF SHELL EGGS
0
1. The authority citation for 21 CFR part 118 continues to read as
follows:
Authority: 21 U.S.C. 321, 331-334, 342, 371, 381, 393; 42 U.S.C.
243, 264, 271.
0
2. In Sec. 118.11, revise paragraphs (a), (b)(2)(i), and (b)(3)(vi) to
read as follows:
Sec. 118.11 Registration requirements for shell egg producers covered
by the requirements of this part.
(a) Shell egg producers covered under Sec. 118.1(a) are required
to register their farms with FDA within 30 days of becoming an egg
producer or, if already an egg producer, by each farm's applicable
compliance date.
(b) * * *
(2) * * *
(i) You must register using FDA Form No. 3733. You may obtain a
copy of this form by writing to the U.S. Food and Drug Administration,
5600 Fishers Lane (HFS-681), Rockville, MD 20857, or by requesting the
form by phone at 1-800-216-7331 or 301-575-0156.
* * * * *
(3) * * *
(vi) You must mail the CD-ROM to the U.S. Food and Drug
Administration, 5600 Fishers Lane (HFS-681), Rockville, MD 20857.
* * * * *
Dated: April 7, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-8358 Filed 4-12-10; 8:45 am]
BILLING CODE 4160-01-S
