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Voluntary Malfunction Summary Reporting (VMSR) Program for Manufacturers: Draft Guidance for Industry and Food and Drug Administration Staff
Information
Type
Guidance
Regulated products
Biologics, Medical Devices
Published
December 9, 2022
Last updated
December 8, 2022
Description
This document is a draft guidance for the Voluntary Malfunction Summary Reporting (VMSR) Program for Manufacturers by the FDA.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)