FDA Inspection 1026172 — Zhejiang Biomet Medical Products Co. Ltd.
The FDA completed an inspection of Zhejiang Biomet Medical Products Co. Ltd. on August 17, 2017 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
- August 17, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jinhua (China)