FDA Inspection 1140939 — GE Parallel Design Inc

GE Parallel Design Inc — FEI 3003309342

The FDA completed an inspection of GE Parallel Design Inc on March 30, 2021 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
March 30, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Postmarket Audit Inspections