FDA Inspection 1060183 — Trinity Medical Center-IRB

Trinity Medical Center-IRB — FEI 3002814154

The FDA completed an inspection of Trinity Medical Center-IRB on Jul 27, 2018 in Rock Island, IL. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rock Island, IL (United States)

Additional Details

IRB

Citations

IDCFRDescription
733721 CFR 56.115(b)Retention of records