FDA Inspection 1000599 - Eurofins MWG Operon, LLC - December 15, 2016

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Record Details

This FDA Inspection record concerns Eurofins MWG Operon, LLC, with an inspection on December 15, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eurofins MWG Operon, LLC
Inspection Date: December 15, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 778f0b26-4c21-4fe6-83ed-100b1284319b

Violation Codes2

21 CFR 820.198(b)21 CFR 820.90(a)

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