FDA Inspection 826247 — TriHealth IRB

TriHealth IRB — FEI 1523743

The FDA completed an inspection of TriHealth IRB on Apr 8, 2013 in Cincinnati, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 8, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cincinnati, OH (United States)

Additional Details

IRB

Citations

IDCFRDescription
727721 CFR 56.107(d)One non-affiliate member