FDA Inspection
GE Medical Systems Information TechnologiesGE Medical Systems Information Technologies – FDA Inspection, Jul 20, 2009
Record Details
This FDA Inspection record concerns GE Medical Systems Information Technologies, with an inspection on July 20, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 20, 2009
- Product Type
- Devices
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ID · da60a1d2-05dd-4600-aa60-60eb50cb2065
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 598985
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.25(b)Training records
- 21 CFR 820.50(a)(3)Acceptable supplier records
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Other FDA inspections of GE Medical Systems Information Technologies
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 28, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 14, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for GE Medical Systems Information Technologies
- FDA Inspection 972198 - 2016-04-28
- FDA Inspection 834140 - 2013-05-14
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