FDA Inspection 920219 — Zhejiang Kindly Medical Devices Co., Ltd.
The FDA completed an inspection of Zhejiang Kindly Medical Devices Co., Ltd. on Mar 25, 2015 in Wenzhou. 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
- Mar 25, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Wenzhou (China)