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FDA Inspection 810120 — Kansas City Fertility Laboratories, LLC

Kansas City Fertility Laboratories, LLC — FEI 3021907345

The FDA completed an inspection of Kansas City Fertility Laboratories, LLC on December 11, 2012 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
December 11, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Wichita, KS (United States)

Facility

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FDA data resources