Home / Inspections / 989459

FDA Inspection 989459 — Envoy Medical Corporation

Envoy Medical Corporation — FEI 3004007782

The FDA completed an inspection of Envoy Medical Corporation on October 27, 2016 in Saint Paul, 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
October 27, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

Facility

Other inspections at this facility

  • 1276707 (OAI Wed Jul 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1163848 (NAI Tue Feb 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1042731 (NAI Wed Feb 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 894694 (VAI Thu Sep 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 713353 (VAI Fri Mar 11 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources