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COMPLIANCE POLICY GUIDE (CPG)

CPG Sec. 300.200 - Reconditioners/Rebuilders of Medical Devices - Revoked-Deletion 01/04/2000 January 2000

Final

Revocation/Deletion

REVOKED January 24, 2000 per Federal Register dated December 23, 1999

Issued: 12/29/87
Revised: 3/95
Revoked January 4, 1999


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Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All comments should be identified with the title of the guidance.