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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 822 - PART 822—POSTMARKET SURVEILLANCE
Subpart A [§ 822.1 - § 822.4] - Subpart A—General Provisions
Subpart B [§ 822.5 - § 822.7] - Subpart B—Notification
Subpart C [§ 822.8 - § 822.15] - Subpart C—Postmarket Surveillance Plan
Subpart D [§ 822.16 - § 822.23] - Subpart D—FDA Review and Action
Subpart E [§ 822.24 - § 822.28] - Subpart E—Responsibilities of Manufacturers
Subpart F [§ 822.29 - § 822.30] - Subpart F—Waivers and Exemptions
Subpart G [§ 822.31 - § 822.38] - Subpart G—Records and Reports
authority:
21 U.S.C. 331
,
352
,
360i
,
360l
,
371
,
374
source:
67 FR 38887, June 6, 2002, unless otherwise noted.
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