CFR 21-803.50-2014
Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.50:If I am a manufacturer, what reporting requirements apply to me?

Standard No.

CFR 21-803.50-2014

Release Date

2014

Published By

US-CFR-file

Latest

CFR 21-803.50-2014

Scope

(a) If you are a manufacturer, you must report to us the information required by § 803.52 in accordance with the requirements of § 803.12(a), no later than 30 calendar days after the day that you receive or otherwise become aware of information, from any

CFR 21-803.50-2014 history

• 2014 CFR 21-803.50-2014 Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.50:If I am a manufacturer, what reporting requirements apply to me?