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Rule

Medical Use of Byproduct Material-Minor Corrections and Clarifications

Document Details

Information about this document as published in the Federal Register.

Published Document

This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.

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AGENCY:

Nuclear Regulatory Commission.

ACTION:

Direct final rule: Confirmation of effective date.

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.

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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: eml1@nrc.gov).

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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 Start Printed Page 54208govern 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.

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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.

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[FR Doc. E7-18743 Filed 9-21-07; 8:45 am]

BILLING CODE 7590-01-P