FDA Inspection 1115560 - Genicon, Inc. - January 17, 2020

Record Details

This FDA Inspection record concerns Genicon, Inc., with an inspection on January 17, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company: Genicon, Inc.
Inspection Date: January 17, 2020
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a21d65bc-f713-40dc-b86a-c87b4c7bb75b

Violation Codes10

21 CFR 803.17(a)(2)21 CFR 803.50(a)(1)21 CFR 803.50(a)(2)21 CFR 806.10(a)(2)21 CFR 820.100(a)21 CFR 820.160(a)21 CFR 820.198(a)21 CFR 820.20(b)21 CFR 820.30(f)21 CFR 820.30(g)

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