FDA Inspection 1020251 - Kreyenberg Gmbh - May 11, 2017

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Record Details

This FDA Inspection record concerns Kreyenberg Gmbh, with an inspection on May 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kreyenberg Gmbh
Inspection Date: May 11, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 856bb98f-2ecf-4bd2-a0c0-8d870911efca

Violation Codes3

21 CFR 820.100(b)21 CFR 820.20(c)21 CFR 820.70(a)

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