21 C.F.R. § 810.1 Scope.
Title 21 - Food and Drugs
Part 810 describes the procedures that the Food and Drug Administration will follow in exercising its medical device recall authority under section 518(e) of the Federal Food, Drug, and Cosmetic Act.
Title 21: Food and Drugs
PART 810—MEDICAL DEVICE RECALL AUTHORITY
Subpart A—General Provisions
§ 810.1 Scope.
