FDA Inspection 863242 - Vetter Pharma Fertigung GmbH & Co. KG - December 05, 2013

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Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG, with an inspection on December 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vetter Pharma Fertigung GmbH & Co. KG
Inspection Date: December 5, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a29a64fc-2b7f-4a0f-ab35-7a5c0d5f996f

Violation Codes1

21 CFR 820.100(a)

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