FDA Inspection 1017586 — Sanimax USA LLC
The FDA completed an inspection of Sanimax USA LLC on June 28, 2017 in South Saint Paul, 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
- June 28, 2017
- Fiscal Year
- 2017
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- South Saint Paul, MN (United States)