FDA Inspection 971669 — Agila Corporation

Agila Corporation — FEI 3008447003

The FDA completed an inspection of Agila Corporation on May 24, 2016 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 24, 2016
Fiscal Year
2016
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Minneapolis, MN (United States)