# FDA Inspection 957490 - Neusoft Medical Systems Co., Ltd. - January 29, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/neusoft-medical-systems-co-ltd/f9cc141b-5edc-4fab-8bf9-6095244bce8a/
Source feed: FDA_Inspections

> FDA Inspection 957490 for Neusoft Medical Systems Co., Ltd. on January 29, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 957490
- Company Name: Neusoft Medical Systems Co., Ltd.
- Inspection Date: 2016-01-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/neusoft-medical-systems-co-ltd/57ea37ca-5a5e-45e4-b66a-6abaa6cb3abd

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