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FDA Inspection 822156 — Saint Luke's Hospital of Kansas City

Saint Luke's Hospital of Kansas City — FEI 1970696

The FDA completed an inspection of Saint Luke's Hospital of Kansas City on March 13, 2013 in Kansas City, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 13, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kansas City, MO (United States)

Facility

Other inspections at this facility

  • 1275693 (NAI Wed Jun 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1163560 (NAI Mon Feb 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1045890 (NAI Wed Feb 28 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 962359 (NAI Wed Mar 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 884528 (NAI Wed Jun 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources