[Federal Register Volume 72, Number 184 (Monday, September 24, 2007)]
[Rules and Regulations]
[Pages 54207-54208]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E7-18743]
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NUCLEAR REGULATORY COMMISSION
10 CFR Parts 32 and 35
RIN 3150-AI14
Medical Use of Byproduct Material--Minor Corrections and
Clarifications
AGENCY: Nuclear Regulatory Commission.
ACTION: Direct final rule: Confirmation of effective date.
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SUMMARY: The Nuclear Regulatory Commission (NRC) is confirming the
effective date of October 29, 2007, for the direct final rule that was
published in the Federal Register on August 13, 2007 (72 FR 45147).
This direct final rule amended the NRC's regulations to correct or
clarify the rule language in several sections in the regulations that
govern specific domestic licenses to manufacture or transfer certain
items containing byproduct material and medical use of byproduct
material.
DATES: The effective date of October 29, 2007 is confirmed for this
direct final rule.
ADDRESSES: Documents related to this rulemaking, including comments
received, may be examined at the NRC Public Document Room, Room O-1F23,
11555 Rockville Pike, Rockville, MD 20852. These same documents are
available electronically at the NRC's Electronic Reading Room at http://www.nrc.gov/NRC/reading-rm/adams.html. From this site, the public can
gain entry into ADAMS, which provides text and image files of NRC's
public documents. If you do not have access to ADAMS or if there are
problems in accessing the documents located in ADAMS, contact the PDR
Reference staff at 1-800-397-4209, 301-415-4737.
FOR FURTHER INFORMATION CONTACT: Edward M. Lohr, Office of Federal and
State Materials and Environmental Management Programs, U.S. Nuclear
Regulatory Commission, Washington, DC 20555, telephone (301) 415-0253
(e-mail: [email protected]).
SUPPLEMENTARY INFORMATION: On August 13, 2007 (72 FR 45147), the NRC
published in the Federal Register a direct final rule amending its
regulations in 10 CFR Parts 32 and 35 to correct or clarify the rule
language in several sections in the regulations that
[[Page 54208]]
govern specific domestic licenses to manufacture or transfer certain
items containing byproduct material and medical use of byproduct
material. In the direct final rule, NRC stated that if no significant
adverse comments were received, the direct final rule would become
final on October 29, 2007. The NRC did not receive any comments that
warranted withdrawal of the direct final rule. Therefore, this rule
will become effective as scheduled.
Dated at Rockville, Maryland, this 18th day of September, 2007.
For the Nuclear Regulatory Commission.
Michael T. Lesar,
Chief, Rulemaking, Directives and Editing Branch, Division of
Administrative Services, Office of Administration.
[FR Doc. E7-18743 Filed 9-21-07; 8:45 am]
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