FDA Inspection 701609 — St Luke's Hospital Of Kansas City

St Luke's Hospital Of Kansas City — FEI 3005059679

The FDA completed an inspection of St Luke's Hospital Of Kansas City on Dec 13, 2010 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 13, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Kansas City, MO (United States)