FDA Inspection 1072268 — Epien Medical, Inc

Epien Medical, Inc — FEI 3003428492

The FDA completed an inspection of Epien Medical, Inc on Nov 1, 2018 in White Bear Lake, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 1, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
White Bear Lake, MN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.