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FDA Inspection
•GE OEC Medical Systems, Inc•June 22, 2018

GE OEC Medical Systems, Inc – FDA Inspection, Jun 22, 2018

Record Details

This FDA Inspection record concerns GE OEC Medical Systems, Inc, with an inspection on June 22, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
GE OEC Medical Systems, Inc
Inspection Date
June 22, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Phillip M. Pontikos (FDA Associated Person)
  • Vicky L. Cruz (FDA Associated Person)
View Company Profile

ID · b4199713-ff26-45fd-b1eb-50f7646f495e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1056985
FDA center
Medical Devices & Rad Health
Project area
Radiation Control and Health Safety Act
Outcome
Form 483 issued

Other FDA inspections of GE OEC Medical Systems, Inc

5
DateClassificationOfficeProject area
August 17, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 29, 2021NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
March 25, 2015OAICenter for Devices and Radiological HealthCompliance: Devices
September 28, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 21, 2008VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for GE OEC Medical Systems, Inc
  • FDA Inspection 1217708 - 2023-08-17
  • FDA Inspection 1145789 - 2021-06-29
  • FDA Inspection 920992 - 2015-03-25
  • FDA Inspection 747277 - 2011-09-28
  • FDA Inspection 550334 - 2008-11-21

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