Change of Name; Technical Amendment, 67650-67651 [05-22167]
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67650
Federal Register / Vol. 70, No. 215 / Tuesday, November 8, 2005 / Rules and Regulations
for all federal employees. The cost of
any life insurance over the $50,000 limit
for each employee.
(A) Any costs, for the year in which
the wages were paid, of the combined
creditable amount of family health and
life insurance for employees over 120
percent of the ‘‘weighted average’’
yearly family health insurance costs for
all federal employee. The cost of any life
insurance over the $50,000 limit for
each employee.
(B) The cost of any pension benefit
per employee over 3 percent of the
employee’s creditable wages unless the
employee’s wages exceed the maximum
annual creditable annual maximum
creditable wage allowed under the
program (see paragraph (a)(9)(i) of this
section). Employees earning over the
maximum creditable wage allowed
under the program would have a
creditable annual pension benefit of up
to 3 percent of the maximum creditable
wage and wages over 3 percent of the
maximum creditable wage would not be
creditable.
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(b) * * *
(2) ITA–360P ‘‘Certificate of
Entitlement to Secure the Refund of
Duties on Articles that Entered the
Customs Territory of The United State
Duty Paid.’’ This document authorizes
an insular jewelry producer to request
the refund of duties on imports of
articles that entered the customs
territory of the United States duty paid,
with certain exceptions, up to the
specified value of the certificate.
Certificates may be used to obtain duty
refunds only when presented with a
properly executed Form ITA–361P.
(3) ITA–361P ‘‘Request for Refund of
Duties on Articles that Entered the
Customs Territory of the United States
Duty Paid.’’ * * *
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I 8. Section 303.17 is amended by
revising paragraph (b)(6); by
redesignating paragraphs (b)(7) and
(b)(8) as paragraphs (b)(8) and (b)(9);
and by adding a new paragraph (b)(7) to
read as follows:
§ 303.17
Annual jewelry application.
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(b) * * *
(6) Customs, bank, payroll,
production records, and all shipping
records including the importer of record
number and proof of residency, as
requested;
(7) All records pertaining to health
insurance, life insurance and pension
benefits for each employee;
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16:28 Nov 07, 2005
Jkt 208001
9. Section 303.19(c)(1) is revised to
read as follows:
I
§ 303.19 Issuance and use of production
incentive certificates.
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(C) The use and transfer of certificate
entitlements. (1) Insular producers
issued a certificate may request a refund
by executing Form ITA–361P (see
§ 303.16(b)(3)) and the instruction on
the form). After authentication by the
Department of Commerce, Form ITA–
361P may be used to obtain duty
refunds on article that entered the
customs territory of the United States
duty paid. Duties on an article which is
the product of a country with respect to
column 2 rates of duty apply may not
be refunded Articles for which duty
refunds are claimed must have entered
the customs territory of the United
States during the two-year period prior
to the issue date of the certificate or
during the one-year period the
certificate remains valid. Copies of the
appropriate Customs entries must be
provided with the refund request in
order to establish a basis for issuing the
claimed amounts. Certification
regarding drawback claims and
liquidated refunds relating to the
presented entries is required from the
claimant on the form.
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10. In § 303.20:
A. Paragraph (a)(2) is revised;
I B. Paragraph (b)(1)(ii) is amended by
removing ‘‘450,000’’ and adding
‘‘3,533,334’’ in its place;
I C. Paragraph (b)(1)(iii) is amended by
removing ‘‘600,000’’ and adding
‘‘6,766,667’’ in its place; and
I D. Paragraph 303.20(b)(1)(iv) is
amended by removing ‘‘750,000’’ and
adding ‘‘10,000,000’’ in its place.
I
I
§ 303.20
Duty refund.
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(a) * * *
(2) Eighteen month exemption. Any
article of jewelry provided for in HTSUS
heading 7113, assembled in the insular
possessions by a new entrant jewelry
manufacturer shall be treated as a
product of the insular possessions if
such article is entered into the customs
territory of the United States no later
than 18 months after such producer
commences jewelry manufacturing or
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Fmt 4700
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jewelry assembly operations in the
insular possessions.
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Joseph A. Spetrini,
Acting Assistant Secretary for Import
Administration, Department of Commerce.
Nikolao I. Pula,
Director for Insular Affairs, Department of
the Interior.
[FR Doc. 05–22244 Filed 11–7–05; 8:45 am]
BILLING CODE 3510–DS–P; 4310–93–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Chapter I
[Docket No. 2005N–0419]
Change of Name; Technical
Amendment
AGENCY:
Food and Drug Administration,
HHS.
Final rule; technical
amendment.
ACTION:
SUMMARY: The Food and Drug
Administration (FDA) is amending its
regulations to reflect a change in the
name for AOAC INTERNATIONAL.
This action is editorial in nature and is
intended to improve the accuracy of the
agency’s regulations.
DATES: This rule is effective November
8, 2005.
FOR FURTHER INFORMATION CONTACT:
Joyce Strong, Office of Policy and
Planning (HF–27), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–7010.
SUPPLEMENTARY INFORMATION: This
document amends FDA’s regulations to
reflect the name change of AOAC
INTERNATIONAL by removing the
outdated name wherever it appears and
by adding the new name in its place in
21 CFR parts 2, 10, 101, 102, 106, 114,
130, 131, 133, 135, 136, 137, 139, 145,
146, 150, 155, 156, 160, 161, 163, 164,
166, 168, 169, 172, 173, 176, 177, 178,
184, 189, 211, 226, 520, and 573.
Publication of this document
constitutes final action on these changes
under the Administrative Procedure Act
(5 U.S.C. 553). Notice and public
procedure are unnecessary because FDA
is merely correcting nonsubstantive
errors.
I Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs, 21 CFR chapter I is
amended as follows:
E:\FR\FM\08NOR1.SGM
08NOR1
Federal Register / Vol. 70, No. 215 / Tuesday, November 8, 2005 / Rules and Regulations
Chapter I [Nomenclature changes]
1. Parts 2, 10, 101, 102, 106, 114, 130,
131, 133, 135, 136, 137, 139, 145, 146,
150, 155, 156, 160, 161, 163, 164, 166,
168, 169, 172, 173, 176, 177, 178, 184,
I
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16:28 Nov 07, 2005
Jkt 208001
189, 211, 226, 520, and 573 are
amended by removing the phrase
‘‘Association of Official Analytical
Chemists International’’ and adding in
its place ‘‘AOAC INTERNATIONAL’’
wherever it appears.
PO 00000
Frm 00011
Fmt 4700
Sfmt 4700
67651
Dated: November 1, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–22167 Filed 11–7–05; 8:45 am]
BILLING CODE 4160–01–S
E:\FR\FM\08NOR1.SGM
08NOR1
]]>Agencies
[Federal Register Volume 70, Number 215 (Tuesday, November 8, 2005)]
[Rules and Regulations]
[Pages 67650-67651]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-22167]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Chapter I
[Docket No. 2005N-0419]
Change of Name; 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 reflect a change in the name for AOAC INTERNATIONAL.
This action is editorial in nature and is intended to improve the
accuracy of the agency's regulations.
DATES: This rule is effective November 8, 2005.
FOR FURTHER INFORMATION CONTACT: Joyce Strong, Office of Policy and
Planning (HF-27), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-7010.
SUPPLEMENTARY INFORMATION: This document amends FDA's regulations to
reflect the name change of AOAC INTERNATIONAL by removing the outdated
name wherever it appears and by adding the new name in its place in 21
CFR parts 2, 10, 101, 102, 106, 114, 130, 131, 133, 135, 136, 137, 139,
145, 146, 150, 155, 156, 160, 161, 163, 164, 166, 168, 169, 172, 173,
176, 177, 178, 184, 189, 211, 226, 520, and 573.
Publication of this document constitutes final action on these
changes under the Administrative Procedure Act (5 U.S.C. 553). Notice
and public procedure are unnecessary because FDA is merely correcting
nonsubstantive errors.
0
Therefore, under the Federal Food, Drug, and Cosmetic Act and under
authority delegated to the Commissioner of Food and Drugs, 21 CFR
chapter I is amended as follows:
[[Page 67651]]
Chapter I [Nomenclature changes]
0
1. Parts 2, 10, 101, 102, 106, 114, 130, 131, 133, 135, 136, 137, 139,
145, 146, 150, 155, 156, 160, 161, 163, 164, 166, 168, 169, 172, 173,
176, 177, 178, 184, 189, 211, 226, 520, and 573 are amended by removing
the phrase ``Association of Official Analytical Chemists
International'' and adding in its place ``AOAC INTERNATIONAL'' wherever
it appears.
Dated: November 1, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05-22167 Filed 11-7-05; 8:45 am]
BILLING CODE 4160-01-S
