FDA Inspection 985171 — Zhejiang Ruibang Laboratories Co., Ltd
The FDA completed an inspection of Zhejiang Ruibang Laboratories Co., Ltd on Jul 21, 2016 in Wenzhou. 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
- Jul 21, 2016
- Fiscal Year
- 2016
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Wenzhou (China)