FDA Inspection 615565 — Saint Luke's Health System

Saint Luke's Health System — FEI 3007844016

The FDA completed an inspection of Saint Luke's Health System on Sep 18, 2009 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 18, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Kansas City, MO (United States)