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FDA Inspection 1080994 — Coloplast Manufacturing US, LLC

Coloplast Manufacturing US, LLC — FEI 2125050

The FDA completed an inspection of Coloplast Manufacturing US, LLC on February 6, 2019 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 6, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
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))
  • 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