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FDA Inspection 1035086 — Gibson Laboratories, LLC

Gibson Laboratories, LLC — FEI 1050138

The FDA completed an inspection of Gibson Laboratories, LLC on November 2, 2017 in Lexington, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 2, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)

Facility

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  • 859677 (VAI Thu Dec 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 659193 (NAI Thu Apr 29 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 610286 (OAI Mon Sep 14 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources