FDA Inspection 548132 - Genicon, Inc. - November 07, 2008

Record Details

This FDA Inspection record concerns Genicon, Inc., with an inspection on November 7, 2008, issued by the Center for Devices and Radiological Health, covering devices.

Company: Genicon, Inc.
Inspection Date: November 7, 2008
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 25e0288c-38ba-4e8f-8af3-eb1086c19256

Violation Codes4

21 CFR 820.100(a)(4)21 CFR 820.30(g)21 CFR 820.50(a)21 CFR 820.75(a)

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