ML20150E450

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Informs of No Legal Objection to Substance of Proposed Rule Re Misadminstration Rept,Per 880205 Request
ML20150E450
Person / Time
Issue date: 02/11/1988
From: Rich Smith
NRC OFFICE OF THE GENERAL COUNSEL (OGC)
To: Mcelroy N
NRC OFFICE OF NUCLEAR MATERIAL SAFETY & SAFEGUARDS (NMSS)
Shared Package
ML20150E436 List:
References
FRN-53FR21627, RULE-PR-35 AC69-2-5, NUDOCS 8807150147
Download: ML20150E450 (4)


Text

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NOTE TO: Norm McElroy IMAB, NMSS FROM: Ron Smith OCC

SUBJECT:

FEDERAL REGISTER NOTICE -

DIAGNOSTIC MISADMINISTRATION REPORT FORM As requested by you on Februarv 5, 1988, I have reviewed the proposed Federal Register notice concerning the above subject and find no legal objection to the substance of the final rule. However, I would note some deficiencies in form as follows:

1. As you intend to make the rule immediately effective upon publication and without public comment, a justification for that action is required.

See section 5.9(f), NUREG/BR-0053, Rev. 1, November 1987, Regulations Handbook. However, none of the examples provided therein appear to apply to this situation and the comment in your final rule on this issue does not appear to be appropriate. Therefore, it is suggested that the following statement be 8ncluded in the Supplementary Section:

"This amendment is a minor administrative change to an existing final rule. It merely adds the form number for an NRC form to the ccdUled rule. The number had been omitted because OMB had not completed its review. Based on this, good cause exists to find that the notice and public procedure provisions of the Administrative Procedure Act are unnecessary pursuant to the exemption provision found in 5 U.S.C. 553(b)(B). Therefore, the amendment is effective upon publicatica in the Federal Register."

2. Within the categorical exclusion for an environmental statement, the reference to paragraph (c)(14) is unnecessary and should be deleted.

The words "for this final rule" should be added at the end of the

. statement.

3. The Regulatory Analysis, Regulatory Flexibility Act, and Backfit Analysis statements have not been included as required by the Regulations Handbook. (However, I can see where they don't necessarily appear to be appropriate. You may wish to discuss these matters,with Rules and Records Division to see if there is a compromise or exception option available under this circumstance.)

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4. .There is a typographical error in the List of Subjects- section in that "Health devices" should read "Health facilities."
5. The words of issuance- under the section Regulatory Text are not in conformance with section. 5.25 of the Regulations Handbook.
6. The Authority citation must include the whole authority citation as it now reads, i.e., the sections issued under authority of 9 223, AEA.

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