FDA Inspection 555756 — A-dec Inc

A-dec Inc — FEI 3015729

The FDA completed an inspection of A-dec Inc on January 7, 2009 in Newberg, OR. 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
January 7, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Newberg, OR (United States)