FDA Inspection 1045088 — Peyman Saadat MD, Inc.

Peyman Saadat MD, Inc. — FEI 3006501117

The FDA completed an inspection of Peyman Saadat MD, Inc. on Mar 21, 2018 in West Hollywood, 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). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 21, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
West Hollywood, CA (United States)

Citations

IDCFRDescription
1222921 CFR 1271.50(a)Determination based on screening and testing
1224721 CFR 1271.55(d)(2)Accurate, indelible, legible

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