FDA Inspection 721471 — Louisville Reproductive Center

Louisville Reproductive Center — FEI 3005081370

The FDA completed an inspection of Louisville Reproductive Center on March 4, 2011 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 4, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Louisville, KY (United States)