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FDA Inspection 1068220 — Coloplast Manufacturing US, LLC

Coloplast Manufacturing US, LLC — FEI 2125050

The FDA completed an inspection of Coloplast Manufacturing US, LLC on September 14, 2018 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
September 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Minneapolis, MN (United States)

Facility

Other inspections at this facility

  • 1307530 (NAI Fri Mar 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 997753 (NAI Wed Nov 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources