80 FR 56369 - Implementation of the Australia Group (AG) November 2013 Intersessional Decisions; Correction

DEPARTMENT OF COMMERCE
Bureau of Industry and Security

Federal Register Volume 80, Issue 181 (September 18, 2015)

Page Range		56369-56370
FR Document		2015-23500

The Bureau of Industry and Security (BIS) publishes this final rule to correct typographical errors contained in a final rule published on June 16, 2015 (80 FR 34266), which amended the Export Administration Regulations (EAR) to implement the recommendations presented at the November 2013 Australia Group (AG) intersessional implementation meeting and later adopted pursuant to the AG silent approval procedure. The typographical errors appear in a Note to ECCN 1C351.a, which includes viruses identified on the AG ``List of Human and Animal Pathogens and Toxins for Export Control.'' This rule also identifies another typographical error in the June 16, 2015, final rule involving the ``Reason for Control'' paragraph for ECCN 1E351. This error does not require a correction at this time, but is being identified to provide clarification to the public.

Federal Register, Volume 80 Issue 181 (Friday, September 18, 2015)

[Federal Register Volume 80, Number 181 (Friday, September 18, 2015)]
[Rules and Regulations]
[Pages 56369-56370]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2015-23500]



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Rules and Regulations
                                                Federal Register
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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. 
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Federal Register / Vol. 80, No. 181 / Friday, September 18, 2015 / 
Rules and Regulations

[[Page 56369]]



DEPARTMENT OF COMMERCE

Bureau of Industry and Security

15 CFR Part 774

[Docket No. 141229999-5828-02]
RIN 0694-AG45


Implementation of the Australia Group (AG) November 2013 
Intersessional Decisions; Correction

AGENCY: Bureau of Industry and Security, Commerce.

ACTION: Correcting amendments.

-----------------------------------------------------------------------

SUMMARY: The Bureau of Industry and Security (BIS) publishes this final 
rule to correct typographical errors contained in a final rule 
published on June 16, 2015 (80 FR 34266), which amended the Export 
Administration Regulations (EAR) to implement the recommendations 
presented at the November 2013 Australia Group (AG) intersessional 
implementation meeting and later adopted pursuant to the AG silent 
approval procedure. The typographical errors appear in a Note to ECCN 
1C351.a, which includes viruses identified on the AG ``List of Human 
and Animal Pathogens and Toxins for Export Control.'' This rule also 
identifies another typographical error in the June 16, 2015, final rule 
involving the ``Reason for Control'' paragraph for ECCN 1E351. This 
error does not require a correction at this time, but is being 
identified to provide clarification to the public.

DATES: This rule is effective September 18, 2015.

FOR FURTHER INFORMATION CONTACT: Richard P. Duncan, Ph.D., Director, 
Chemical and Biological Controls Division, Office of Nonproliferation 
and Treaty Compliance, Bureau of Industry and Security, Telephone: 
(202) 482-3343, Email: Richard.Duncan@bis.doc.gov.

SUPPLEMENTARY INFORMATION: 
    On June 16, 2015, the Bureau of Industry and Security (BIS) 
published the final rule ``Implementation of the Australia Group (AG) 
November 2013 Intersessional Decisions'' (80 FR 34266), which amended 
the Export Administration Regulations (EAR) to reflect the merger of 
two AG common control lists by removing ECCN 1C352 (animal pathogens) 
from the CCL and adding the pathogens previously controlled under ECCN 
1C352 to ECCN 1C351 (human and zoonotic pathogens and ``toxins''). The 
latter ECCN was renamed to indicate that it controls both human and 
animal pathogens and ``toxins.'' That final rule also renumbered the 
items in ECCN 1C351.a, and certain items in ECCN 1C351.c to accommodate 
the addition to ECCN 1C351 of those items that had been controlled 
under ECCN 1C352 prior to the publication of that rule.
    As amended by the June 16, 2015, final rule, the Note to ECCN 
1C351.a.4 (which controls avian influenza viruses identified as having 
high pathogenicity) incorrectly referenced ECCN 1C352.a.4, instead of 
ECCN 1C351.a.4. This final rule corrects the references contained in 
that Note. Specifically, the Note to ECCN 1C351.a.4 is corrected to 
read as follows: ``Avian influenza (AI) viruses of the H5 or H7 subtype 
that do not have either of the characteristics described in 1C351.a.4 
(specifically, 1C351.a.4.a or a.4.b) should be sequenced to determine 
whether multiple basic amino acids are present at the cleavage site of 
the haemagglutinin molecule (HA0). If the amino acid motif is similar 
to that observed for other HPAI isolates, then the isolate being tested 
should be considered as HPAI and the virus is controlled under 
1C351.a.4.'' The corrections to this Note do not affect the scope of 
the controls described in ECCN 1C351.a.4.
    In addition, the text for ECCN 1E351, as published in the June 16, 
2015, final rule incorrectly identified the applicable controls for 
this ECCN under the ``Reason for Control'' paragraph in the License 
Requirements section. Specifically, the ``Reason for Control'' 
paragraph mistakenly identified the applicable controls for ECCN 1E351 
as ``NS, MT, NP, CB, RS, AT,'' instead of ``CB, AT.'' It is not 
necessary, however, to amend ECCN 1E351 to correct this error, because 
the amendatory instructions for ECCN 1E351 in the June 16, 2015, final 
rule did not include a specific instruction to amend the ``Reason for 
Control'' paragraph for this ECCN. Consequently, the ``Reason for 
Control'' paragraph in ECCN 1E351 was not revised by the June 16, 2015, 
final rule. The paragraph, as published in the CCL, continues to 
correctly identify the applicable controls for this ECCN as ``CB, AT.'' 
BIS identifies this error to inform the public of the inconsistency 
between the contents of the June 16, 2015, final rule and the CCL, and 
to provide clarification regarding the applicable controls for ECCN 
1E351.
    Although the Export Administration Act expired on August 20, 2001, 
the President, through Executive Order 13222 of August 17, 2001, 3 CFR, 
2001 Comp., p. 783 (2002), as amended by Executive Order 13637 of March 
8, 2013, 78 FR 16129 (March 13, 2013), and as extended by the Notice of 
August 7, 2015 (80 FR 48,233 (Aug. 11, 2015)), has continued the Export 
Administration Regulations in effect under the International Emergency 
Economic Powers Act. BIS continues to carry out the provisions of the 
Export Administration Act, as appropriate and to the extent permitted 
by law, pursuant to Executive Order 13222, as amended by Executive 
Order 13637.

Rulemaking Requirements

    1. Executive Orders 13563 and 12866 direct agencies to assess all 
costs and benefits of available regulatory alternatives and, if 
regulation is necessary, to select regulatory approaches that maximize 
net benefits (including potential economic, environmental, public 
health and safety effects, distributive impacts, and equity). Executive 
Order 13563 emphasizes the importance of quantifying both costs and 
benefits, of reducing costs, of harmonizing rules, and of promoting 
flexibility. This rule has been determined to be not significant for 
purposes of Executive Order 12866.
    2. Notwithstanding any other provision of law, no person is 
required to respond to, nor shall any person be subject to a penalty 
for failure to comply with, a collection of information subject to the 
requirements of the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et 
seq.) (PRA), unless that collection of information displays a currently 
valid

[[Page 56370]]

Office of Management and Budget (OMB) Control Number. This rule 
contains a collection of information subject to the requirements of the 
PRA. This collection has been approved by OMB under Control Number 
0694-0088 (Multi-Purpose Application), which carries a burden hour 
estimate of 58 minutes to prepare and submit form BIS-748. Send 
comments regarding this burden estimate or any other aspect of this 
collection of information, including suggestions for reducing the 
burden, to Jasmeet Seehra, Office of Management and Budget (OMB), and 
to the Regulatory Policy Division, Bureau of Industry and Security, 
Department of Commerce, 14th Street & Pennsylvania Avenue NW., Room 
2705, Washington, DC 20230.
    3. This rule does not contain policies with Federalism implications 
as that term is defined in Executive Order 13132.
    4. The provisions of the Administrative Procedure Act (5 U.S.C. 
553) requiring notice of proposed rulemaking and the opportunity for 
public participation are waived for good cause because they are 
unnecessary and contrary to the public interest. (See 5 U.S.C. 
553(b)(B)). The changes contained in this rule are non-substantive 
technical corrections of a previously published rule that has already 
been exempted from notice and comment. This rule is necessary to ensure 
clarity in the regulations and accuracy regarding the scope of controls 
in the Note to ECCN 1C351.a.4. If this rule were delayed to allow for 
notice and comment, it would result in further confusion caused by the 
incorrect cross-references in that ECCN. These changes are also 
essential to ensuring the accurate and complete implementation of the 
June 16, 2015, final rule.
    The provision of the Administrative Procedure Act (5 U.S.C. 553) 
requiring a 30-day delay in effectiveness is also waived for good 
cause. (5 U.S.C. 553(d)(3)). The corrections contained in this final 
rule are non-substantive technical corrections of a previously 
published rule that has already been exempted from notice and comment. 
If this rule were delayed to allow for a 30-day delay in effectiveness, 
it would result in further confusion caused by the incorrect cross-
references in the aforementioned ECCN. These changes are also essential 
to ensuring the accurate and complete implementation of the June 16, 
2015, final rule.
    Further, no other law requires that a notice of proposed rulemaking 
and an opportunity for public comment be given for this final rule. 
Because a notice of proposed rulemaking and an opportunity for public 
comment are not required to be given for this rule under the 
Administrative Procedure Act or by any other law, the analytical 
requirements of the Regulatory Flexibility Act (5 U.S.C. 601 et seq.) 
are not applicable. Therefore, this regulation is issued in final form.

List of Subjects in 15 CFR Part 774

    Exports, Reporting and recordkeeping requirements.

    For the reasons stated in the preamble, part 774 of the Export 
Administration Regulations (15 CFR parts 730-774) is amended as 
follows:

PART 774--[AMENDED]

0
1. The authority citation for 15 CFR part 774 continues to read as 
follows:

    Authority: 50 U.S.C. app. 2401 et seq.; 50 U.S.C. 1701 et seq.; 
10 U.S.C. 7420; 10 U.S.C. 7430(e); 22 U.S.C. 287c, 22 U.S.C. 3201 et 
seq.; 22 U.S.C. 6004; 30 U.S.C. 185(s), 185(u); 42 U.S.C. 2139a; 42 
U.S.C. 6212; 43 U.S.C. 1354; 15 U.S.C. 1824a; 50 U.S.C. app. 5; 22 
U.S.C. 7201 et seq.; 22 U.S.C. 7210; E.O. 13026, 61 FR 58767, 3 CFR, 
1996 Comp., p. 228; E.O. 13222, 66 FR 44025, 3 CFR, 2001 Comp., p. 
783; Notice of August 7, 2015 (80 FR 48233 (Aug. 11, 2015)).


0
2. In Supplement No. 1 to Part 774 (the Commerce Control List), 
Category 1-- Special Materials and Related Equipment, Chemicals, 
``Microorganisms'' and ``Toxins,'' ECCN 1C351 is amended under the 
``Items'' paragraph in the List of Items Controlled section by revising 
the Note immediately following paragraph a.4.b to read as follows:

Supplement No. 1 to Part 774--the Commerce Control List

* * * * *
1C351 Human and animal pathogens and ``toxins'', as follows (see List 
of Items Controlled).
* * * * *

List of Items Controlled

* * * * *
Items:
    a. * * *
    a.4. * * *
    a.4.b. * * *

    Note: Avian influenza (AI) viruses of the H5 or H7 subtype that 
do not have either of the characteristics described in 1C351.a.4 
(specifically, 1C351.a.4.a or a.4.b) should be sequenced to 
determine whether multiple basic amino acids are present at the 
cleavage site of the haemagglutinin molecule (HA0). If the amino 
acid motif is similar to that observed for other HPAI isolates, then 
the isolate being tested should be considered as HPAI and the virus 
is controlled under 1C351.a.4.

* * * * *

    Dated: September 10, 2015.
Karen H. Nies-Vogel,
Director, Office of Exporter Services.
[FR Doc. 2015-23500 Filed 9-17-15; 8:45 am]
BILLING CODE 3510-33-P

56369

Rules and Regulations Federal Register
Vol. 80, No. 181

Friday, September 18, 2015

This section of the FEDERAL REGISTER SUPPLEMENTARY INFORMATION: instructions for ECCN 1E351 in the June
contains regulatory documents having general On June 16, 2015, the Bureau of 16, 2015, final rule did not include a
applicability and legal effect, most of which Industry and Security (BIS) published specific instruction to amend the
are keyed to and codified in the Code of the final rule ‘‘Implementation of the ‘‘Reason for Control’’ paragraph for this
Federal Regulations, which is published under Australia Group (AG) November 2013 ECCN. Consequently, the ‘‘Reason for
50 titles pursuant to 44 U.S.C. 1510.
Intersessional Decisions’’ (80 FR 34266), Control’’ paragraph in ECCN 1E351 was
The Code of Federal Regulations is sold by which amended the Export not revised by the June 16, 2015, final
the Superintendent of Documents. Prices of Administration Regulations (EAR) to rule. The paragraph, as published in the
new books are listed in the first FEDERAL reflect the merger of two AG common CCL, continues to correctly identify the
REGISTER issue of each week. control lists by removing ECCN 1C352 applicable controls for this ECCN as
(animal pathogens) from the CCL and ‘‘CB, AT.’’ BIS identifies this error to
adding the pathogens previously inform the public of the inconsistency
DEPARTMENT OF COMMERCE controlled under ECCN 1C352 to ECCN between the contents of the June 16,
1C351 (human and zoonotic pathogens 2015, final rule and the CCL, and to
Bureau of Industry and Security and ‘‘toxins’’). The latter ECCN was provide clarification regarding the
renamed to indicate that it controls both applicable controls for ECCN 1E351.
15 CFR Part 774 human and animal pathogens and Although the Export Administration
[Docket No. 141229999–5828–02] ‘‘toxins.’’ That final rule also Act expired on August 20, 2001, the
renumbered the items in ECCN 1C351.a, President, through Executive Order
RIN 0694–AG45
and certain items in ECCN 1C351.c to 13222 of August 17, 2001, 3 CFR, 2001
Implementation of the Australia Group accommodate the addition to ECCN Comp., p. 783 (2002), as amended by
(AG) November 2013 Intersessional 1C351 of those items that had been Executive Order 13637 of March 8,
Decisions; Correction controlled under ECCN 1C352 prior to 2013, 78 FR 16129 (March 13, 2013),
the publication of that rule. and as extended by the Notice of August
AGENCY: Bureau of Industry and As amended by the June 16, 2015, 7, 2015 (80 FR 48,233 (Aug. 11, 2015)),
Security, Commerce. final rule, the Note to ECCN 1C351.a.4 has continued the Export
ACTION: Correcting amendments. (which controls avian influenza viruses Administration Regulations in effect
identified as having high pathogenicity) under the International Emergency
SUMMARY: The Bureau of Industry and incorrectly referenced ECCN 1C352.a.4, Economic Powers Act. BIS continues to
Security (BIS) publishes this final rule instead of ECCN 1C351.a.4. This final carry out the provisions of the Export
to correct typographical errors rule corrects the references contained in Administration Act, as appropriate and
contained in a final rule published on that Note. Specifically, the Note to to the extent permitted by law, pursuant
June 16, 2015 (80 FR 34266), which ECCN 1C351.a.4 is corrected to read as to Executive Order 13222, as amended
amended the Export Administration follows: ‘‘Avian influenza (AI) viruses of by Executive Order 13637.
Regulations (EAR) to implement the the H5 or H7 subtype that do not have
recommendations presented at the Rulemaking Requirements
either of the characteristics described in
November 2013 Australia Group (AG) 1C351.a.4 (specifically, 1C351.a.4.a or 1. Executive Orders 13563 and 12866
intersessional implementation meeting a.4.b) should be sequenced to determine direct agencies to assess all costs and
and later adopted pursuant to the AG whether multiple basic amino acids are benefits of available regulatory
silent approval procedure. The present at the cleavage site of the alternatives and, if regulation is
typographical errors appear in a Note to haemagglutinin molecule (HA0). If the necessary, to select regulatory
ECCN 1C351.a, which includes viruses amino acid motif is similar to that approaches that maximize net benefits
identified on the AG ‘‘List of Human observed for other HPAI isolates, then (including potential economic,
and Animal Pathogens and Toxins for the isolate being tested should be environmental, public health and safety
Export Control.’’ This rule also considered as HPAI and the virus is effects, distributive impacts, and
identifies another typographical error in controlled under 1C351.a.4.’’ The equity). Executive Order 13563
the June 16, 2015, final rule involving corrections to this Note do not affect the emphasizes the importance of
the ‘‘Reason for Control’’ paragraph for scope of the controls described in ECCN quantifying both costs and benefits, of
ECCN 1E351. This error does not require 1C351.a.4. reducing costs, of harmonizing rules,
a correction at this time, but is being In addition, the text for ECCN 1E351, and of promoting flexibility. This rule
identified to provide clarification to the as published in the June 16, 2015, final has been determined to be not
public. rule incorrectly identified the applicable significant for purposes of Executive
DATES: This rule is effective September controls for this ECCN under the Order 12866.
18, 2015. ‘‘Reason for Control’’ paragraph in the 2. Notwithstanding any other
FOR FURTHER INFORMATION CONTACT: License Requirements section. provision of law, no person is required
Richard P. Duncan, Ph.D., Director, Specifically, the ‘‘Reason for Control’’ to respond to, nor shall any person be
tkelley on DSK3SPTVN1PROD with RULES

Chemical and Biological Controls paragraph mistakenly identified the subject to a penalty for failure to comply
Division, Office of Nonproliferation and applicable controls for ECCN 1E351 as with, a collection of information subject
Treaty Compliance, Bureau of Industry ‘‘NS, MT, NP, CB, RS, AT,’’ instead of to the requirements of the Paperwork
and Security, Telephone: (202) 482– ‘‘CB, AT.’’ It is not necessary, however, Reduction Act of 1995 (44 U.S.C. 3501
3343, Email: Richard.Duncan@ to amend ECCN 1E351 to correct this et seq.) (PRA), unless that collection of
bis.doc.gov. error, because the amendatory information displays a currently valid

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56370 Federal Register / Vol. 80, No. 181 / Friday, September 18, 2015 / Rules and Regulations

Office of Management and Budget opportunity for public comment are not Dated: September 10, 2015.
(OMB) Control Number. This rule required to be given for this rule under Karen H. Nies-Vogel,
contains a collection of information the Administrative Procedure Act or by Director, Office of Exporter Services.
subject to the requirements of the PRA. any other law, the analytical [FR Doc. 2015–23500 Filed 9–17–15; 8:45 am]
This collection has been approved by requirements of the Regulatory BILLING CODE 3510–33–P
OMB under Control Number 0694–0088 Flexibility Act (5 U.S.C. 601 et seq.) are
(Multi-Purpose Application), which not applicable. Therefore, this
carries a burden hour estimate of 58 regulation is issued in final form. DEPARTMENT OF HOMELAND
minutes to prepare and submit form
List of Subjects in 15 CFR Part 774 SECURITY
BIS–748. Send comments regarding this
burden estimate or any other aspect of Exports, Reporting and recordkeeping U.S. Customs and Border Protection
this collection of information, including requirements.
suggestions for reducing the burden, to For the reasons stated in the DEPARTMENT OF THE TREASURY
Jasmeet Seehra, Office of Management preamble, part 774 of the Export
and Budget (OMB), and to the Administration Regulations (15 CFR 19 CFR Parts 133 and 151
Regulatory Policy Division, Bureau of parts 730–774) is amended as follows:
Industry and Security, Department of [Docket No. USCBP–2012–0011; CBP Dec.
Commerce, 14th Street & Pennsylvania PART 774—[AMENDED] 15–12]
Avenue NW., Room 2705, Washington, RIN 1515–AD87
DC 20230. ■ 1. The authority citation for 15 CFR
3. This rule does not contain policies part 774 continues to read as follows: Disclosure of Information for Certain
with Federalism implications as that Authority: 50 U.S.C. app. 2401 et seq.; 50 Intellectual Property Rights Enforced
term is defined in Executive Order U.S.C. 1701 et seq.; 10 U.S.C. 7420; 10 U.S.C. at the Border
13132. 7430(e); 22 U.S.C. 287c, 22 U.S.C. 3201 et
4. The provisions of the seq.; 22 U.S.C. 6004; 30 U.S.C. 185(s), 185(u); AGENCIES: U.S. Customs and Border
Administrative Procedure Act (5 U.S.C. 42 U.S.C. 2139a; 42 U.S.C. 6212; 43 U.S.C. Protection, Department of Homeland
553) requiring notice of proposed 1354; 15 U.S.C. 1824a; 50 U.S.C. app. 5; 22 Security; Department of the Treasury.
U.S.C. 7201 et seq.; 22 U.S.C. 7210; E.O.
rulemaking and the opportunity for ACTION: Final rule.
13026, 61 FR 58767, 3 CFR, 1996 Comp., p.
public participation are waived for good 228; E.O. 13222, 66 FR 44025, 3 CFR, 2001
cause because they are unnecessary and SUMMARY: This document adopts as a
Comp., p. 783; Notice of August 7, 2015 (80
contrary to the public interest. (See 5 final rule, with changes, interim
FR 48233 (Aug. 11, 2015)).
U.S.C. 553(b)(B)). The changes amendments to the U.S. Customs and
■ 2. In Supplement No. 1 to Part 774 Border Protection (CBP) regulations
contained in this rule are non- (the Commerce Control List), Category
substantive technical corrections of a pertaining to importations of
1— Special Materials and Related merchandise bearing suspected
previously published rule that has
Equipment, Chemicals, counterfeit trademarks or trade names
already been exempted from notice and
‘‘Microorganisms’’ and ‘‘Toxins,’’ ECCN that are recorded with CBP. Specifically,
comment. This rule is necessary to
1C351 is amended under the ‘‘Items’’ the amendments allow CBP, for the
ensure clarity in the regulations and
paragraph in the List of Items Controlled purpose of obtaining assistance in
accuracy regarding the scope of controls
section by revising the Note determining whether merchandise bears
in the Note to ECCN 1C351.a.4. If this
immediately following paragraph a.4.b a counterfeit mark, to disclose to a
rule were delayed to allow for notice
to read as follows: trademark or other mark owner
and comment, it would result in further
confusion caused by the incorrect cross- Supplement No. 1 to Part 774—the information appearing on merchandise
references in that ECCN. These changes Commerce Control List or its retail packaging that may
are also essential to ensuring the otherwise be protected by the Trade
* * * * * Secrets Act. This final rule also amends
accurate and complete implementation 1C351 Human and animal pathogens
of the June 16, 2015, final rule. the CBP regulations to further enhance
and ‘‘toxins’’, as follows (see List of information-sharing procedures by
The provision of the Administrative
Items Controlled). requiring CBP to release to the importer
Procedure Act (5 U.S.C. 553) requiring
a 30-day delay in effectiveness is also * * * * * an unredacted sample or image of the
waived for good cause. (5 U.S.C. List of Items Controlled suspect merchandise or its retail
553(d)(3)). The corrections contained in packaging any time after presentation of
this final rule are non-substantive * * * * * the suspect goods for examination. This
Items: change is to reflect that an importer may
technical corrections of a previously a. * * *
published rule that has already been a.4. * * * not have complete information about
exempted from notice and comment. If a.4.b. * * * the marks appearing on imported goods,
this rule were delayed to allow for a 30- and release of such unredacted
Note: Avian influenza (AI) viruses of the information will assist the importer in
day delay in effectiveness, it would H5 or H7 subtype that do not have either of
result in further confusion caused by the the characteristics described in 1C351.a.4
providing CBP with a meaningful
incorrect cross-references in the (specifically, 1C351.a.4.a or a.4.b) should be response to a detention notice. The
aforementioned ECCN. These changes sequenced to determine whether multiple amendments in this final rule also
are also essential to ensuring the basic amino acids are present at the cleavage require CBP to release limited
accurate and complete implementation site of the haemagglutinin molecule (HA0). If importation information to the mark
tkelley on DSK3SPTVN1PROD with RULES

of the June 16, 2015, final rule. the amino acid motif is similar to that owner no later than the time of issuance
Further, no other law requires that a observed for other HPAI isolates, then the of the detention notice to the importer,
notice of proposed rulemaking and an isolate being tested should be considered as rather than within 30 business days
HPAI and the virus is controlled under
opportunity for public comment be 1C351.a.4.
from the date of detention. Finally,
given for this final rule. Because a these amendments require CBP to notify
notice of proposed rulemaking and an * * * * * the mark owner that use of any

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Document Created: 2015-12-15 09:27:31
Document Modified: 2015-12-15 09:27:31

Category		Regulatory Information
Collection		Federal Register
sudoc Class		AE 2.7: GS 4.107: AE 2.106:
Publisher		Office of the Federal Register, National Archives and Records Administration
Section		Rules and Regulations
Action		Correcting amendments.
Dates		This rule is effective September 18, 2015.
Contact		Richard P. Duncan, Ph.D., Director, Chemical and Biological Controls Division, Office of Nonproliferation and Treaty Compliance, Bureau of Industry and Security, Telephone: (202) 482-3343, Email: [email protected]
FR Citation		80 FR 56369
RIN Number		0694-AG45
CFR Associated		Exports and Reporting and Recordkeeping Requirements

80 FR 56369 - Implementation of the Australia Group (AG) November 2013 Intersessional Decisions; Correction

DEPARTMENT OF COMMERCEBureau of Industry and Security

Federal Register Volume 80, Issue 181 (September 18, 2015)

DEPARTMENT OF COMMERCE
Bureau of Industry and Security