# Suzhou KD Intelligent Device Co., Ltd – FDA Inspection, Jul 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 of Suzhou KD Intelligent Device Co., Ltd, July 25, 2024. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 801, 803 and 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- FDA Inspection 984322 - 2016-06-16

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

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