FDA Inspection 1013135 - Audifon Gmbh - May 11, 2017

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Record Details

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

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

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ID · 091f3f59-75b8-4501-9e1e-feaca250b850

Violation Codes9

21 CFR 803.17(a)(2)21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.18421 CFR 820.30(e)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.5021 CFR 820.75(a)

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