CFR 21-803.56-2014
Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.56:If I am a manufacturer, in what circumstances must I submit a supplemental or followup report and what are the requirements for such reports?

Standard No.
CFR 21-803.56-2014
Release Date
2014
Published By
US-CFR-file
Latest
CFR 21-803.56-2014
Scope
If you are a manufacturer, when you obtain information required under this part that you did not provide because it was not known or was not available when you submitted the initial report, you must submit the supplemental information to us within 30 cale

CFR 21-803.56-2014 history

  • 2014 CFR 21-803.56-2014 Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.56:If I am a manufacturer, in what circumstances must I submit a supplemental or followup report and what are the requirements for such reports?



Copyright ©2024 All Rights Reserved