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FDA Inspection 1323476 — Kansas City Fertility Laboratories, LLC

Kansas City Fertility Laboratories, LLC — FEI 3021907345

The FDA completed an inspection of Kansas City Fertility Laboratories, LLC on June 10, 2026 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
June 10, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Wichita, KS (United States)

Facility

Other inspections at this facility

  • 1216492 (NAI Tue Aug 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 993637 (NAI Tue Nov 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 920573 (NAI Thu Apr 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810120 (NAI Tue Dec 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 743120 (NAI Mon Sep 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources