FDA Inspection 997339 - Corflex, Inc. - January 04, 2017

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Record Details

This FDA Inspection record concerns Corflex, Inc., with an inspection on January 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Corflex, Inc.
Inspection Date: January 4, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 740c9446-a019-4be3-acc1-754b81c2337a

Violation Codes2

21 CFR 803.1721 CFR 820.198(a)

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