FDA Inspection 698574 - Weinmann Gmbh - October 21, 2010

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Record Details

This FDA Inspection record concerns Weinmann Gmbh, with an inspection on October 21, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Weinmann Gmbh
Inspection Date: October 21, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b744f097-2293-41b1-9c57-462ca8cb949d

Violation Codes2

21 CFR 820.70(i)21 CFR 820.75(c)

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