FDA Inspection 1115222 — Venus Concept Inc

Venus Concept Inc — FEI 3006515340

The FDA completed an inspection of Venus Concept Inc on January 16, 2020 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 16, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
San Jose, CA (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
369621 CFR 820.100(b)Documentation