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