FDA Inspection 662181 — Midwest Protein

Midwest Protein — FEI 3004777812

The FDA completed an inspection of Midwest Protein on May 10, 2010 in Grove City, MN. 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
May 10, 2010
Fiscal Year
2010
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Grove City, MN (United States)