FDA Inspection 645167 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3003253380

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Jan 27, 2010 in Pasadena, 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 27, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Pasadena, CA (United States)

Citations

IDCFRDescription
1222121 CFR 1271.47(a)Procedures for all other requirements

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