Amends the Federal Food, Drug, and Cosmetic Act to require manufacturers, importers, and distributors of medical devices to maintain…
Official title: A bill to amend the Federal Food, Drug, and Cosmetic Act to require manufacturers, importers, and distributors of medical devices to maintain certain records respecting the handling of complaints, analysis of device failures, and the return of devices.
This bill died when its Congress ended.
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Amends the Federal Food, Drug, and Cosmetic Act to require manufacturers, importers, and distributors of medical devices to maintain certain records respecting procedures for the handling of complaints, analysis of device failures, and the return of devices.
Filed in the House
This house bill has been filed and is working its way through Congress. It will need to pass both the House and the Senate, then be signed by the President to become law.
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