CFR 21-803.30-2014
Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.30:If I am a user facility, what reporting requirements apply to me?

Standard No.

CFR 21-803.30-2014

Release Date

2014

Published By

US-CFR-file

Latest

CFR 21-803.30-2014

Scope

(a) You must submit reports to the manufacturer or to us, or both, as specified in paragraphs (a)(1) and (a)(2) of this section as follows:

CFR 21-803.30-2014 history

• 2014 CFR 21-803.30-2014 Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.30:If I am a user facility, what reporting requirements apply to me?