FDA Inspection 1014720 — Venus Concept Inc

Venus Concept Inc — FEI 3006515340

The FDA completed an inspection of Venus Concept Inc on May 2, 2017 in San Jose, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures
367121 CFR 820.25(a)Personnel