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FDA Inspection 951146 — Coloplast Manufacturing US, LLC

Coloplast Manufacturing US, LLC — FEI 2125050

The FDA completed an inspection of Coloplast Manufacturing US, LLC on November 24, 2015 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
November 24, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Minneapolis, MN (United States)

Facility

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  • 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