Home / Inspections / 759709

FDA Inspection 759709 — Coloplast Manufacturing US, LLC

Coloplast Manufacturing US, LLC — FEI 2125050

The FDA completed an inspection of Coloplast Manufacturing US, LLC on December 14, 2011 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
December 14, 2011
Fiscal Year
2012
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))
  • 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))

FDA data resources