FDA Inspection 761103 — Huntington Reproductive Center Medical Group

Huntington Reproductive Center Medical Group — FEI 3005108085

The FDA completed an inspection of Huntington Reproductive Center Medical Group on Dec 22, 2011 in Westlake Village, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 22, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Westlake Village, CA (United States)