FDA Inspection 1278618 — Shenzhen Kentro Medical Electronics Co., Ltd.
The FDA completed an inspection of Shenzhen Kentro Medical Electronics Co., Ltd. on August 15, 2025 in Shenzhen. 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 15, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)