FDA Inspection 959637 - Spiegelberg Gmbh & Co. KG - February 04, 2016

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Record Details

This FDA Inspection record concerns Spiegelberg Gmbh & Co. KG, with an inspection on February 4, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Spiegelberg Gmbh & Co. KG
Inspection Date: February 4, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5c7e2179-f422-472d-a073-762d5d12cbfa

Violation Codes10

21 CFR 803.1721 CFR 803.50(a)(2)21 CFR 803.53(a)21 CFR 806.10(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.250(b)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.50

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