FDA Inspection 913071 — Zhejiang Biomet Medical Products Co. Ltd.
The FDA completed an inspection of Zhejiang Biomet Medical Products Co. Ltd. on January 22, 2015 in Jinhua. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- January 22, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jinhua (China)