FDA Inspection 1115222 - Venus Concept Inc - January 16, 2020

FDA Inspection 1115222 for Venus Concept Inc on January 16, 2020. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1115222 for Venus Concept Inc on January 16, 2020. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

21 CFR 820.198(a)

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Record Information

Company

Venus Concept Inc

Inspection Date

January 16, 2020

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 52c7d570-f75e-4071-8320-17e8b4cd281d

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