# GE Medical Systems Information Technologies – FDA Inspection, Jul 20, 2009

Source: https://www.keypedia.com/records/fda_inspections/ge-medical-systems-information-technologies/da60a1d2-05dd-4600-aa60-60eb50cb2065
Source feed: FDA_Inspections

> FDA inspection 598985 of GE Medical Systems Information Technologies, July 20, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598985
- Company Name: GE Medical Systems Information Technologies
- Inspection Date: 2009-07-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 972198 - 2016-04-28
- FDA Inspection 834140 - 2013-05-14

Company: https://www.keypedia.com/companies/ge-medical-systems-information-technologies/adbe506e-3c82-4e7a-a8ed-4ac018cb8c0f

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