Business · 26/01/2000Updated: 10/17/2026 · 1 min read
FDA Announces Collection of Information for Medical Device Manufacturers for Review Under Paperwork Reduction Act
Summary
The Food and Drug Administration (FDA) is seeking public comment on proposed reporting and recordkeeping requirements for medical device manufacturers, importers, user facilities, and distributors, as part of the Paperwork Reduction Act of 1995 review process
Original source language: Federal Register — Food and Drug AdministrationOpen original release →