FDA Inspection 882603 — Zhejiang Gongdong Medical Technology Co., Ltd
The FDA completed an inspection of Zhejiang Gongdong Medical Technology Co., Ltd on May 22, 2014 in Taizhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 22, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Taizhou (China)