# Shenzhen Dongdixin Technology Co., Ltd. – FDA Inspection, Sep 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-dongdixin-technology-co-ltd/464f917e-fd15-4e8d-aaf3-c291a73cfefa
Source feed: FDA_Inspections

> FDA inspection 1026108 of Shenzhen Dongdixin Technology Co., Ltd., September 06, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026108
- Company Name: Shenzhen Dongdixin Technology Co., Ltd.
- Inspection Date: 2017-09-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/shenzhen-dongdixin-technology-co-ltd/2329a09b-a618-476d-b4d7-bde091644070

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