FDA Inspection 1294476 — Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.

Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. — FEI 3006545436

The FDA completed an inspection of Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. on October 31, 2025 in Taizhou. 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
October 31, 2025
Fiscal Year
2026
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Taizhou (China)