# FDA Inspection 1026108 - Shenzhen Dongdixin Technology Co., Ltd. - September 06, 2017

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

> FDA Inspection 1026108 for Shenzhen Dongdixin Technology Co., Ltd. on September 06, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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