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FDA Inspection 859677 — Gibson Laboratories, LLC

Gibson Laboratories, LLC — FEI 1050138

The FDA completed an inspection of Gibson Laboratories, LLC on December 12, 2013 in Lexington, KY. 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
December 12, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)

Facility

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Recent compliance actions

FDA data resources