FDA Inspection 813877 - The Flexite Company - January 09, 2013

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Record Details

This FDA Inspection record concerns The Flexite Company, with an inspection on January 9, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Flexite Company
Inspection Date: January 9, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 107ce64d-e156-4aa6-866e-737143b7b26c

Violation Codes1

21 CFR 803.17(b)(2)

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