FDA Inspection 1240290 — ProMedica Health System IRB

ProMedica Health System IRB — FEI 3000210664

The FDA completed an inspection of ProMedica Health System IRB on April 5, 2024 in Toledo, OH. 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 5, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Toledo, OH (United States)

Additional Details

IRB