FDA Inspection 931562 - Weinmann Gmbh - June 25, 2015

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Record Details

This FDA Inspection record concerns Weinmann Gmbh, with an inspection on June 25, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Weinmann Gmbh
Inspection Date: June 25, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5711be22-1f9b-4a44-97c6-2b010ea3d188

Violation Codes1

21 CFR 820.90(b)(1)

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