FDA Inspection 1076508 - Vioguard, Inc. - January 17, 2019

Record Details

This FDA Inspection record concerns Vioguard, Inc., with an inspection on January 17, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vioguard, Inc.
Inspection Date: January 17, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6a28fef9-d092-4d60-9afb-0d5c05cc757e

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(c)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.30(h)21 CFR 820.40

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