FDA Inspection 1288974 — Zhejiang Kindly Medical Devices Co., Ltd.
The FDA completed an inspection of Zhejiang Kindly Medical Devices Co., Ltd. on Sep 18, 2025 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
- Sep 18, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Wenzhou (China)