FDA Inspection 1068522 — Zhejiang Jiuzhou Pharmaceutical Co., Ltd.
The FDA completed an inspection of Zhejiang Jiuzhou Pharmaceutical Co., Ltd. on September 13, 2018 in Taizhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- September 13, 2018
- Fiscal Year
- 2018
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Taizhou (China)