FDA Inspection 879666 — Venus Concept Inc

Venus Concept Inc — FEI 3006515340

The FDA completed an inspection of Venus Concept Inc on April 22, 2014 in San Jose, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 22, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Jose, CA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
63521 CFR 803.17(b)(1)Info evaluated to determine if event was reportable