FDA Inspection 993637 — Kansas City Fertility Laboratories, LLC

Kansas City Fertility Laboratories, LLC — FEI 3021907345

The FDA completed an inspection of Kansas City Fertility Laboratories, LLC on November 15, 2016 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
November 15, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Wichita, KS (United States)