FDA Inspection 924788 — Louisville Reproductive Center

Louisville Reproductive Center — FEI 3005081370

The FDA completed an inspection of Louisville Reproductive Center on April 30, 2015 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
April 30, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Louisville, KY (United States)