# Unimicro Medical Systems (Shenzhen) Co., Ltd. – FDA Inspection, Nov 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/unimicro-medical-systems-shenzhen-co-ltd/d39b2fc8-f2ef-4624-83af-2fc49bddcc28
Source feed: FDA_Inspections

> FDA inspection 1036153 of Unimicro Medical Systems (Shenzhen) Co., Ltd., November 09, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1036153
- Company Name: Unimicro Medical Systems (Shenzhen) Co., Ltd.
- Inspection Date: 2017-11-09
- 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: 0

## Related Documents

- [FDA Inspection 1199692 - 2023-03-03](https://www.keypedia.com/records/fda_inspections/unimicro-medical-systems-shenzhen-co-ltd/5a129cf6-ffb4-46c8-88f3-f3f55b3bba67)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gregson-a-joseph/90bf8118-3f32-4f44-95c4-fcde1f741a18)

Company: https://www.keypedia.com/companies/unimicro-medical-systems-shenzhen-co-ltd/21c0703f-383f-449c-8a6d-53c7e9f63b32

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