FDA Inspection 932088 — Sioux Pharm Inc

Sioux Pharm Inc — FEI 3002750210

The FDA completed an inspection of Sioux Pharm Inc on Jun 16, 2015 in Sioux Center, IA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 16, 2015
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Sioux Center, IA (United States)