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FDA Inspection 887596 — Ducommun Labarge Technologies

Ducommun Labarge Technologies — FEI 1000139867

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

Facility

Other inspections at this facility

  • 1274180 (VAI Fri Jun 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022305 (VAI Fri Aug 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources