# FDA Inspection 1278618 - Shenzhen Kentro Medical Electronics Co., Ltd. - August 15, 2025

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-kentro-medical-electronics-co-ltd/e69e4e1b-337e-44cb-8b85-9e384e4f78f6
Source feed: FDA_Inspections

> FDA Inspection 1278618 for Shenzhen Kentro Medical Electronics Co., Ltd. on August 15, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1278618
- Company Name: Shenzhen Kentro Medical Electronics Co., Ltd.
- Inspection Date: 2025-08-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1278618 - 2025-08-15](https://www.keypedia.com/records/fda_inspections/shenzhen-kentro-medical-electronics-co-ltd/bb82b4d0-a381-4104-8d1c-8ca332c61429)
- [FDA Inspection 1278618 - 2025-08-15](https://www.keypedia.com/records/fda_inspections/shenzhen-kentro-medical-electronics-co-ltd/85bf170f-7c34-41d0-be4e-d54f544c2dc8)

Company: https://www.keypedia.com/companies/shenzhen-kentro-medical-electronics-co-ltd/0e79a0ab-1941-491e-877b-32020be11d0c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7