FDA Inspection 991776 — George King Bio-Medical, Inc.

George King Bio-Medical, Inc. — FEI 1928890

The FDA completed an inspection of George King Bio-Medical, Inc. on Oct 27, 2016 in Overland Park, KS. 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
Oct 27, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Overland Park, KS (United States)

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