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FDA Inspection 1024888 — GE Parallel Design Inc

GE Parallel Design Inc — FEI 3003309342

The FDA completed an inspection of GE Parallel Design Inc on August 10, 2017 in Phoenix, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Phoenix, AZ (United States)

Facility

Other inspections at this facility

  • 1140939 (NAI Tue Mar 30 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821449 (NAI Tue Feb 26 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources