FDA Inspection 852293 - Bredent GmbH & Co. KG - September 19, 2013

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Record Details

This FDA Inspection record concerns Bredent GmbH & Co. KG, with an inspection on September 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bredent GmbH & Co. KG
Inspection Date: September 19, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ed3df42e-b3b3-4463-9b3d-9ba85e6ffa0d

Violation Codes1

21 CFR 820.70(i)

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