FDA Inspection 1288066 — Zhejiang Shenzhou Pharmaceutical Co., Ltd.

Zhejiang Shenzhou Pharmaceutical Co., Ltd. — FEI 3005463252

The FDA completed an inspection of Zhejiang Shenzhou Pharmaceutical Co., Ltd. on Sep 12, 2025 in Taizhou. 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
Sep 12, 2025
Fiscal Year
2025
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Taizhou (China)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.