CFR 21-806.10-2013
Food and Drugs. Part806:Medical devices; reports of corrections and removals. Section806.10:Reports of corrections and removals.

Standard No.

CFR 21-806.10-2013

Release Date

2013

Published By

US-CFR-file

Latest

CFR 21-806.10-2013

Scope

(a) Each device manufacturer or importer shall submit a written report to FDA of any correction or removal of a device initiated by such manufacturer or importer if the correction or removal was initiated:

CFR 21-806.10-2013 history

• 2013 CFR 21-806.10-2013 Food and Drugs. Part806:Medical devices; reports of corrections and removals. Section806.10:Reports of corrections and removals.