CFR 21-830.120-2013
Food and Drugs. Part830:Unique device identification. Section830.120:Responsibilities of an FDA-accredited issuing agency.

Standard No.

CFR 21-830.120-2013

Release Date

2013

Published By

US-CFR-file

Latest

CFR 21-830.120-2013

Scope

To maintain its accreditation, an issuing agency must:

CFR 21-830.120-2013 history

• 2013 CFR 21-830.120-2013 Food and Drugs. Part830:Unique device identification. Section830.120:Responsibilities of an FDA-accredited issuing agency.