FDA Inspection 1004520 — Facemaster of Beverly Hills, Inc.

Facemaster of Beverly Hills, Inc. — FEI 3008726571

The FDA completed an inspection of Facemaster of Beverly Hills, Inc. on February 28, 2017 in Canoga Park, 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
February 28, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Canoga Park, CA (United States)

Citations

IDCFRDescription
1472021 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation