FDA Inspection 1102731 - DynaFlex - September 05, 2019

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Record Details

This FDA Inspection record concerns DynaFlex, with an inspection on September 5, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: DynaFlex
Inspection Date: September 5, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0226fb05-c7a0-4f3a-a4db-17fc00be71c8