FDA Inspection 924001 — 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 April 21, 2015 in Pontiac, MI. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 21, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Pontiac, MI (United States)

Additional Details

IRB