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FDA Inspection 1072268 — Epien Medical, Inc

Epien Medical, Inc — FEI 3003428492

The FDA completed an inspection of Epien Medical, Inc on November 1, 2018 in White Bear Lake, 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
November 1, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
White Bear Lake, MN (United States)

Facility

Other inspections at this facility

  • 1280917 (VAI Thu Aug 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1247073 (NAI Tue Aug 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1073560 (VAI Thu Dec 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859099 (VAI Wed Dec 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 730791 (NAI Wed Jun 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources