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FDA Inspection 743120 — Kansas City Fertility Laboratories, LLC

Kansas City Fertility Laboratories, LLC — FEI 3021907345

The FDA completed an inspection of Kansas City Fertility Laboratories, LLC on September 12, 2011 in Wichita, KS. 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
September 12, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Wichita, KS (United States)

Facility

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FDA data resources