FDA Inspection 887596 — Ducommun Labarge Technologies

Ducommun Labarge Technologies — FEI 1000139867

The FDA completed an inspection of Ducommun Labarge Technologies on Jul 17, 2014 in Appleton, WI. 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
Jul 17, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Appleton, WI (United States)

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