FDA Inspection 1068392 - The Flexite Company - October 05, 2018

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Record Details

This FDA Inspection record concerns The Flexite Company, with an inspection on October 5, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Flexite Company
Inspection Date: October 5, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8337315f-a3be-42d4-aa02-63fd2611af12