21 CFR Part 822 - POSTMARKET SURVEILLANCE
- SUBPART A — General Provisions (§§ 822.1 - 822.4)
- SUBPART B — Notification (§§ 822.5 - 822.7)
- SUBPART C — Postmarket Surveillance Plan (§§ 822.8 - 822.15)
- SUBPART D — FDA Review and Action (§§ 822.16 - 822.23)
- SUBPART E — Responsibilities of Manufacturers (§§ 822.24 - 822.28)
- SUBPART F — Waivers and Exemptions (§§ 822.29 - 822.30)
- SUBPART G — Records and Reports (§§ 822.31 - 822.38)
Source:
67 FR 38887, June 6, 2002, unless otherwise noted.
Title 21 published on 2014-04-01
no entries appear in the Federal Register after this date.