Revisions to Labeling Requirements for Blood and Blood Components, Including Source Plasma; Correction, 6463 [2012-2828]
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6463
Rules and Regulations
Federal Register
Vol. 77, No. 26
Wednesday, February 8, 2012
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.
Correction to Final Rule
DATES:
Accordingly, pursuant to the
authority delegated to me, the legal
description as published in the Federal
Register on January 3, 2012 (77 FR 6),
(FR Doc. 2011–33566), is corrected as
follows:
2012.
§ 71.1
[Amended]
AAL AK E5
Kwigillingok, AK [Corrected]
On page 7, column 2, and line 50 of
the legal description, remove ‘‘Lat.
59°32′35″ N.,’’ and insert ‘‘Lat. 59°52′35″
N.,’’ and on line 52 remove ‘‘within a
6.5-mile radius * * *’’ and insert
‘‘within a 6.6-mile radius * * *’’.
■
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 71
[Docket No. FAA–2011–0881; Airspace
Docket No. 11–AAL–18]
Issued in Seattle, Washington, on January
27, 2012.
Robert Henry,
Acting Manager, Operations Support Group,
Western Service Center.
Amendment of Class E Airspace;
Kwigillingok, AK
Federal Aviation
Administration (FAA), DOT.
ACTION: Final rule, correction.
AGENCY:
[FR Doc. 2012–2764 Filed 2–7–12; 8:45 am]
BILLING CODE 4910–13–P
This action corrects a final
rule published in the Federal Register
of January 3, 2012 that amends Class E
airspace at Kwigillingok Airport,
Kwigillingok, AK. In that rule, errors
were made in the geographic
coordinates and legal description for
Kwigillingok Airport. This action
corrects these errors.
DATES: Effective Date: 0901 UTC, April
5, 2012. The Director of the Federal
Register approves this incorporation by
reference action under 1 CFR Part 51,
subject to the annual revision of FAA
Order 7400.9 and publication of
conforming amendments.
FOR FURTHER INFORMATION CONTACT:
Jeanette Roller, Federal Aviation
Administration, Operations Support
Group, Western Service Center, 1601
Lind Avenue SW., Renton, WA 98057;
telephone (425) 203–4541.
SUPPLEMENTARY INFORMATION:
pmangrum on DSK3VPTVN1PROD with RULES
SUMMARY:
History
On January 3, 2012, a final rule for
Airspace Docket No. 11–AAL–18, FAA
Docket No. FAA–2011–0881 was
published in the Federal Register (77
FR 6), amending controlled airspace at
Kwigillingok Airport, AK. Subsequent
to publication, an error was found in the
latitude coordinate for Kwigillingok
Airport, and the radius referencing Class
E 700 foot airspace. This action corrects
these errors.
VerDate Mar<15>2010
14:44 Feb 07, 2012
Jkt 226001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
This rule is effective July 2,
FOR FURTHER INFORMATION CONTACT:
Joyce Strong, Office of Policy, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 32, rm. 3208,
Silver Spring, MD 20993–0002, (301)
796–9148.
SUPPLEMENTARY INFORMATION: In the FR
Doc. 2011–33554, appearing on page 7
in the Federal Register of Tuesday,
January 3, 2012 (77 FR 7), the following
correction is made:
1. On page 15, in the third column, in
the third full paragraph, the first
sentence is corrected to read: ‘‘To
comply with section 3506(c)(2)(A) of the
PRA (44 U.S.C. 3506(c)(2)(A)), FDA
published a notice of proposed
collection of information on December
30, 2011.’’ We are making this change
because the notice of proposed
collection inadvertently did not publish
on January 3, 2012.
Dated: February 2, 2012.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2012–2828 Filed 2–7–12; 8:45 am]
BILLING CODE 4160–01–P
21 CFR Parts 606, 610, and 640
[Docket No. FDA–2003–N–0097; Formerly
2003N–0211]
Revisions to Labeling Requirements
for Blood and Blood Components,
Including Source Plasma; Correction
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final rule; correction.
The Food and Drug
Administration (FDA) is correcting a
final rule that appeared in the Federal
Register of January 3, 2012. In the
Federal Register of January 3, 2012,
FDA published a final rule entitled
‘‘Revisions to Labeling Requirements for
Blood and Blood Components,
Including Source Plasma,’’ which
provided incorrect publication
information regarding a 60-day notice
that announced the availability of an
opportunity for public comment on the
proposed collection of certain
information by FDA pertaining to the
final rule. This document corrects this
error. Elsewhere in this issue of the
Federal Register, FDA is publishing a
companion 60-day correction notice.
SUMMARY:
PO 00000
Frm 00001
Fmt 4700
Sfmt 4700
DEPARTMENT OF THE TREASURY
Office of Foreign Assets Control
31 CFR Parts 543, 546, and 547
Definition of the Term ‘‘Financial,
Material, or Technological Support’’
ˆ
Under the Cote d’Ivoire, Darfur, and
Democratic Republic of the Congo
Sanctions Regulations
Office of Foreign Assets
Control, Treasury.
ACTION: Final rule.
AGENCY:
The Department of the
Treasury’s Office of Foreign Assets
ˆ
Control (‘‘OFAC’’) is amending the Cote
d’Ivoire Sanctions Regulations, the
Darfur Sanctions Regulations, and the
Democratic Republic of the Congo
Sanctions Regulations to add a
definition of the term ‘‘financial,
material, or technological support’’ as
used in these regulations. Providing
‘‘financial, material, or technological
support’’ for, inter alia, any person
whose property and interests in
property are blocked under those
regulations constitutes one of the
SUMMARY:
E:\FR\FM\08FER1.SGM
08FER1
]]>Agencies
[Federal Register Volume 77, Number 26 (Wednesday, February 8, 2012)]
[Rules and Regulations]
[Page 6463]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2828]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 606, 610, and 640
[Docket No. FDA-2003-N-0097; Formerly 2003N-0211]
Revisions to Labeling Requirements for Blood and Blood
Components, Including Source Plasma; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is correcting a final
rule that appeared in the Federal Register of January 3, 2012. In the
Federal Register of January 3, 2012, FDA published a final rule
entitled ``Revisions to Labeling Requirements for Blood and Blood
Components, Including Source Plasma,'' which provided incorrect
publication information regarding a 60-day notice that announced the
availability of an opportunity for public comment on the proposed
collection of certain information by FDA pertaining to the final rule.
This document corrects this error. Elsewhere in this issue of the
Federal Register, FDA is publishing a companion 60-day correction
notice.
DATES: This rule is effective July 2, 2012.
FOR FURTHER INFORMATION CONTACT: Joyce Strong, Office of Policy, Food
and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, rm. 3208,
Silver Spring, MD 20993-0002, (301) 796-9148.
SUPPLEMENTARY INFORMATION: In the FR Doc. 2011-33554, appearing on page
7 in the Federal Register of Tuesday, January 3, 2012 (77 FR 7), the
following correction is made:
1. On page 15, in the third column, in the third full paragraph,
the first sentence is corrected to read: ``To comply with section
3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)), FDA published a
notice of proposed collection of information on December 30, 2011.'' We
are making this change because the notice of proposed collection
inadvertently did not publish on January 3, 2012.
Dated: February 2, 2012.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2012-2828 Filed 2-7-12; 8:45 am]
BILLING CODE 4160-01-P
