FDA Inspection
GE Healthcare Japan CorporationGE Healthcare Japan Corporation – FDA Inspection, Sep 15, 2017
Record Details
This FDA Inspection record concerns GE Healthcare Japan Corporation, with an inspection on September 15, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 15, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · e584138a-fb75-4a30-a2de-5ca74734d108
Inspection Facts
- Inspection number
- 1081180
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of GE Healthcare Japan Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 15, 2017 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| May 21, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 5, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for GE Healthcare Japan Corporation
- FDA Inspection 1038779 - 2017-12-15
- FDA Inspection 932420 - 2015-05-21
- FDA Inspection 781576 - 2012-04-05
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