# FDA Inspection 1246231 - Suzhou KD Intelligent Device Co., Ltd - July 25, 2024

Source: https://www.keypedia.com/records/fda_inspections/suzhou-kd-intelligent-device-co-ltd/1c067f21-2a91-48e1-bb74-d9f7b44b2b3e
Source feed: FDA_Inspections

> FDA Inspection 1246231 for Suzhou KD Intelligent Device Co., Ltd on July 25, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1246231
- Company Name: Suzhou KD Intelligent Device Co., Ltd
- Inspection Date: 2024-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1246231 - 2024-07-25](https://www.keypedia.com/records/fda_inspections/suzhou-kd-intelligent-device-co-ltd/0bc53c4a-a60b-423e-b102-f09643e493c1)
- [FDA Inspection 984322 - 2016-06-16](https://www.keypedia.com/records/fda_inspections/suzhou-kd-intelligent-device-co-ltd/6bfaf1ef-3b0d-476e-9e4f-3c59587d45de)

Company: https://www.keypedia.com/companies/suzhou-kd-intelligent-device-co-ltd/16aff6b1-96d4-4ea2-a69e-1c0c0f62751d

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