FDA Inspection 1067024 — Gondra, Maria M, M.D., FACOG

Gondra, Maria M, M.D., FACOG — FEI 3012879844

The FDA completed an inspection of Gondra, Maria M, M.D., FACOG on Sep 21, 2018 in Phoenix, AZ. 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection details

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

Citations

IDCFRDescription
1222921 CFR 1271.50(a)Determination based on screening and testing

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