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 Feb 28, 2017 in Canoga Park, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 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

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