FDA Inspection 1276122 — Trinity Health Michigan Regional IRB #4

Trinity Health Michigan Regional IRB #4 — FEI 1825380

The FDA completed an inspection of Trinity Health Michigan Regional IRB #4 on July 16, 2025 in Pontiac, MI. 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
July 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Pontiac, MI (United States)

Additional Details

IRB