# Neusoft Medical Systems Co., Ltd. – FDA Inspection, Jan 29, 2016

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

> FDA inspection 957490 of Neusoft Medical Systems Co., Ltd., January 29, 2016. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803, 806, 820, 1002 and 1020. 4 other FDA inspections on record for this company.

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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)
- 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: 7

## Related Documents

- FDA Inspection 1083050 - 2019-01-24
- FDA Inspection 957496 - 2016-02-04
- FDA Inspection 844103 - 2013-08-02
- FDA Inspection 667977 - 2010-06-03

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

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