FDA Inspection 1278303 — Sanford Health IRB

Sanford Health IRB — FEI 3008660749

The FDA completed an inspection of Sanford Health IRB on August 11, 2025 in Sioux Falls, SD. 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
August 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Sioux Falls, SD (United States)

Additional Details

IRB