FDA Inspection 938356 — Zhejiang Hisoar Pharmaceutical Co. Ltd.

Zhejiang Hisoar Pharmaceutical Co. Ltd. — FEI 3003735151

The FDA completed an inspection of Zhejiang Hisoar Pharmaceutical Co. Ltd. on August 13, 2015 in Taizhou. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Veterinary.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 13, 2015
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Taizhou (China)