FDA Inspection 1203471 — Essentia Health IRB #1

Essentia Health IRB #1 — FEI 2127620

The FDA completed an inspection of Essentia Health IRB #1 on April 6, 2023 in Duluth, 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
April 6, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Duluth, MN (United States)

Additional Details

IRB