FDA Inspection 880279 — Medpace Medical Device

Medpace Medical Device — FEI 3010838219

The FDA completed an inspection of Medpace Medical Device on May 27, 2014 in Circle Pines, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 27, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Circle Pines, MN (United States)

Additional Details

Sponsor, Contract Research Organization