FEI 1000139867
Ducommun Labarge Technologies
2222 E Pensar Dr, APPLETON, WI, US
MDR events0All time
Recalls0All time
Registered products12
Establishment typeManufactureManufacture Medical Device for Another Party (Contract Manufacturer)
Registered product codes
12 product codes
Recent MDR events
0 on file
No MDR events on file for this firm name.
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 1000139867.
FDA inspections
2 on file
- Voluntary Action Indicated (VAI)Jun 27, 2025
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Jun 27, 2025
Postmarket Assurance: Devices · Citations posted
Inspection citations
4 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.75(a)Jun 27, 2025
Lack of or inadequate process validation
- 21 CFR 820.80(a)Jun 27, 2025
Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.90(a)Jun 27, 2025
Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.100(a)Jun 27, 2025
Lack of or inadequate procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
1 on file
Top refusal reasons
Compare to industry ↗- Division of Northern Border Imports (DNBI)Aug 5, 2026
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