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FDA Inspection 920573 — Kansas City Fertility Laboratories, LLC

Kansas City Fertility Laboratories, LLC — FEI 3021907345

The FDA completed an inspection of Kansas City Fertility Laboratories, LLC on April 2, 2015 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
April 2, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Wichita, KS (United States)

Facility

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  • 993637 (NAI Tue Nov 15 2016 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