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 Mar 13, 2013 in Kansas City, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

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

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