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 NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 22, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Jinhua (China)