FDA Inspection 555756 — A-Dec Inc

A-Dec Inc — FEI 3015729

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.