FDA Inspection 635880 — Neogen Corporation

Neogen Corporation — FEI 3005038302

The FDA completed an inspection of Neogen Corporation on Dec 22, 2009 in Lexington, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 22, 2009
Fiscal Year
2010
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Lexington, KY (United States)

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