# FDA Inspection 1038962 - GE Hangwei Medical Systems, Co. LTD - December 12, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/ge-hangwei-medical-systems-co-ltd/946b86d5-5c02-4b4a-84cf-25112186459c
Source feed: FDA_Inspections

> FDA Inspection 1038962 for GE Hangwei Medical Systems, Co. LTD on December 12, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038962
- Company Name: GE Hangwei Medical Systems, Co. LTD
- Inspection Date: 2017-12-12
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 936991 - 2015-07-30](https://www.globalkeysolutions.net/records/fda_inspections/ge-hangwei-medical-systems-co-ltd/35e3db08-e2d1-43ed-b730-d64acba846b7)
- [FDA Inspection 936991 - 2015-07-30](https://www.globalkeysolutions.net/records/fda_inspections/ge-hangwei-medical-systems-co-ltd/6c670bfd-8874-4701-9c00-f3acb708d083)
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Company: https://www.globalkeysolutions.net/companies/ge-hangwei-medical-systems-co-ltd/51ed20ea-ddd3-462f-b5cb-4153127ca735

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