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