Medical Devices; Immunology and Microbiology Devices; Classification of Norovirus Serological Reagents; Correction, 19534 [2012-7757]
Download as PDF
<![CDATA[
19534
Federal Register / Vol. 77, No. 63 / Monday, April 2, 2012 / Rules and Regulations
public procedure as unnecessary. For
this same reason, pursuant to 5 U.S.C.
553(d)(3), CBP finds that good cause
exists for dispensing with the
requirement for a delayed effective date.
The Regulatory Flexibility Act
Because this document is not subject
to the notice and public procedure
requirements of 5 U.S.C. 553, it is not
subject to the provisions of the
Regulatory Flexibility Act (5 U.S.C. 601
et seq.).
Executive Order 12866
As these amendments are technical
corrections to the regulations to reflect
statutory changes, these amendments do
not meet the criteria for a ‘‘significant
regulatory action’’ as specified in
Executive Order 12866.
Signing Authority
This document is limited to technical
corrections of the CBP regulations.
Accordingly, it is being signed under
the authority of 19 CFR 0.1(b)(1).
List of Subjects
19 CFR Part 171
Administrative practice and
procedure, Customs duties and
inspection, Law enforcement, Penalties,
Seizures and forfeitures.
19 CFR Part 172
Administrative practice and
procedure, Customs duties and
inspection, Penalties.
Amendments to the CBP Regulations
For the reasons stated in the
preamble, parts 171 and 172 of title 19
of the Code of Federal Regulations (19
CFR parts 171 and 172) are amended as
set forth below.
PART 171—FINES, PENALTIES, AND
FORFEITURES
PART 172—CLAIMS FOR LIQUIDATED
DAMAGES; PENALTIES SECURED BY
BONDS
4. The authority citation for part 172
is revised to read as follows:
■
Authority: 19 U.S.C. 66, 1618, 1623, 1624.
§ 172.11
[Amended]
5. Section 172.11(a) is amended by
removing the phrase ‘‘, or section 320 of
title 46, United States Code App. (46
U.S.C. App. 320),’’, and by removing the
word ‘‘shall’’ and adding in its place the
word ‘‘will’’.
■
§ 172.12
[Amended]
6. Section 172.12 is amended by:
a. Removing the phrase ‘‘, or section
320 of title 46, United States Code App.
(46 U.S.C. App. 320),’’;
■ b. Adding the words ‘‘International
Trade, ’’ after the words, ‘‘Office of’’;
and
■ c. Removing the word ‘‘Customs’’ and
adding in its place the term ‘‘CBP’’.
■
■
Dated: March 28, 2012.
David V. Aguilar,
Acting Commissioner, U.S. Customs and
Border Protection.
[FR Doc. 2012–7814 Filed 3–30–12; 8:45 am]
BILLING CODE 9111–14–P
[Amended]
2. Section 171.11(a) is amended by
removing the phrase ‘‘, or section 320 of
title 46, United States Code App. (46
U.S.C. App. 320),’’.
sroberts on DSK5SPTVN1PROD with RULES
[Amended]
VerDate Mar<15>2010
15:38 Mar 30, 2012
Jkt 226001
BILLING CODE 4160–01–P
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
RIN 1625–AA08
Food and Drug Administration
Special Local Regulations; Savannah
Tall Ships Challenge, Savannah River,
Savannah, GA
AGENCY:
ACTION:
Food and Drug Administration,
HHS.
ACTION:
Final rule; correction.
In the Federal Register of
March 9, 2012 (76 FR 14272), the Food
and Drug Administration (FDA)
classified norovirus serological reagents
into class II (special controls) because
special controls, in addition to general
controls, will provide a reasonable
assurance of safety and effectiveness of
PO 00000
Frm 00014
Fmt 4700
Sfmt 4700
Coast Guard, DHS.
Temporary final rule.
AGENCY:
Medical Devices; Immunology and
Microbiology Devices; Classification of
Norovirus Serological Reagents;
Correction
SUMMARY:
3. Section 171.12 is amended by:
a. Adding the word, ‘‘or’’, before the
phrase ‘‘section 5321(c) of title 31,
United States Code (31 U.S.C. 5321(c))’’;
■ b. Removing the phrase ‘‘, or section
320 of title 46, United States Code App.
(46 U.S.C. App. 320),’’;
■
■
[FR Doc. 2012–7757 Filed 3–30–12; 8:45 am]
[Docket No. USCG–2012–0039]
■
§ 171.12
Dated: March 27, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Docket No. FDA–2012–N–0165]
Authority: 18 U.S.C. 983; 19 U.S.C. 66,
1592, 1593a, 1618, 1624; 22 U.S.C. 401; 31
U.S.C. 5321.
these devices. The document published
with inadvertent errors in the Analysis
of Impacts section. This document
corrects those errors.
DATES: Effective April 9, 2012.
FOR FURTHER INFORMATION CONTACT:
Steven Gitterman, Center for Devices
and Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, rm. 5518, Silver Spring,
MD 20993–0002, 301–796–6694.
SUPPLEMENTARY INFORMATION: In FR Doc.
2012–5675 appearing on page 14272 in
the Federal Register of Friday, March 9,
2012, the following corrections are
made:
1. On page 14274, in the first column,
in section VI. Analysis of Impacts, in the
first paragraph, in the last sentence,
correct the phrase ‘‘proposed rule’’ to
read ‘‘final rule’’, and in the second
paragraph, in the last sentence, correct
the phrase ‘‘proposes to certify’’ to read
‘‘certifies’’.
2. On page 14274, in the second
column, in the first full sentence,
correct the phrase ‘‘proposed rule’’ to
read ‘‘final rule’’.
33 CFR Part 100
21 CFR Part 866
1. The authority citation for part 171
is revised to read as follows:
■
§ 171.11
c. Removing the words ‘‘, unless there
has been no delegation to act by the
Secretary of the Treasury or his
designee’’;
■ d. Removing the last sentence of the
paragraph; and
■ e. Adding the punctuation ‘‘.’’ after
the word ‘‘appropriate’’.
■
The Coast Guard is
establishing special local regulations on
the Savannah River in Savannah,
Georgia during the Savannah Tall Ships
Challenge. The Savannah Tall Ships
Challenge will take place from
Thursday, May 3, 2012 through
Monday, May 7, 2012. Approximately
15 vessels are anticipated to participate
in the event. These special local
regulations are necessary to provide for
the safety of life and property on
navigable waters of the United States
during the event. The special local
regulations establish the following three
areas: Mooring zones; buffer zones; and
SUMMARY:
E:\FR\FM\02APR1.SGM
02APR1
]]>Agencies
[Federal Register Volume 77, Number 63 (Monday, April 2, 2012)]
[Rules and Regulations]
[Page 19534]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-7757]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 866
[Docket No. FDA-2012-N-0165]
Medical Devices; Immunology and Microbiology Devices;
Classification of Norovirus Serological Reagents; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; correction.
-----------------------------------------------------------------------
SUMMARY: In the Federal Register of March 9, 2012 (76 FR 14272), the
Food and Drug Administration (FDA) classified norovirus serological
reagents into class II (special controls) because special controls, in
addition to general controls, will provide a reasonable assurance of
safety and effectiveness of these devices. The document published with
inadvertent errors in the Analysis of Impacts section. This document
corrects those errors.
DATES: Effective April 9, 2012.
FOR FURTHER INFORMATION CONTACT: Steven Gitterman, Center for Devices
and Radiological Health, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 66, rm. 5518, Silver Spring, MD 20993-0002, 301-
796-6694.
SUPPLEMENTARY INFORMATION: In FR Doc. 2012-5675 appearing on page 14272
in the Federal Register of Friday, March 9, 2012, the following
corrections are made:
1. On page 14274, in the first column, in section VI. Analysis of
Impacts, in the first paragraph, in the last sentence, correct the
phrase ``proposed rule'' to read ``final rule'', and in the second
paragraph, in the last sentence, correct the phrase ``proposes to
certify'' to read ``certifies''.
2. On page 14274, in the second column, in the first full sentence,
correct the phrase ``proposed rule'' to read ``final rule''.
Dated: March 27, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012-7757 Filed 3-30-12; 8:45 am]
BILLING CODE 4160-01-P
