FDA Inspection
GE Hangwei Medical Systems, Co. LTDGE Hangwei Medical Systems, Co. LTD – FDA Inspection, Sep 22, 2017
Record Details
This FDA Inspection record concerns GE Hangwei Medical Systems, Co. LTD, with an inspection on September 22, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 22, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 968a639b-726d-4d7a-8b75-48f327d94f98
Inspection Facts
- Inspection number
- 1051347
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of GE Hangwei Medical Systems, Co. LTD
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2018 | Not classified | Office of Inspections and Investigations | |
| December 12, 2017 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 22, 2017 | Not classified | Office of Inspections and Investigations | |
| July 30, 2015 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 1, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for GE Hangwei Medical Systems, Co. LTD
- FDA Inspection 1132247 - 2018-09-14
- FDA Inspection 1038962 - 2017-12-12
- FDA Inspection 1060550 - 2017-09-22
- FDA Inspection 936991 - 2015-07-30
- FDA Inspection 749189 - 2011-09-01
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