FDA Inspection 1029478 - Genicon, Inc. - October 20, 2017

Record Details

This FDA Inspection record concerns Genicon, Inc., with an inspection on October 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Genicon, Inc.
Inspection Date: October 20, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 25d492d8-2efe-424d-8840-d1105072458f

Violation Codes5

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.5021 CFR 820.75(a)

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