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FDA Inspection 1307530 — Coloplast Manufacturing US, LLC

Coloplast Manufacturing US, LLC — FEI 2125050

The FDA completed an inspection of Coloplast Manufacturing US, LLC on March 6, 2026 in Minneapolis, MN. 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
March 6, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1196697 (NAI Fri Jan 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1080994 (NAI Wed Feb 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066755 (VAI Tue Sep 25 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1068220 (NAI Fri Sep 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 997753 (NAI Wed Nov 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources