FDA Inspection 996093 - Repro-Med Systems, Inc. - December 16, 2016

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Record Details

This FDA Inspection record concerns Repro-Med Systems, Inc., with an inspection on December 16, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Repro-Med Systems, Inc.
Inspection Date: December 16, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0ac00916-4fe9-4b11-bf62-d3a8ef4a40e1