FDA Inspection
Vioguard, Inc.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.
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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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