FDA Inspection 1238338 — Gibson Laboratories, LLC

Gibson Laboratories, LLC — FEI 1050138

The FDA completed an inspection of Gibson Laboratories, LLC on April 25, 2024 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
April 25, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)