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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 October 27, 2016 in Overland Park, KS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 27, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Overland Park, KS (United States)

Facility

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  • 1024197 (VAI Wed Sep 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 903607 (NAI Thu Nov 13 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources