FDA Inspection 1015906 — ProMedica Health System IRB

ProMedica Health System IRB — FEI 3000210664

The FDA completed an inspection of ProMedica Health System IRB on May 18, 2017 in Toledo, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 18, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Toledo, OH (United States)

Additional Details

IRB