FDA Inspection 998945 — Trinity Health - New England IRB

Trinity Health - New England IRB — FEI 1283390

The FDA completed an inspection of Trinity Health - New England IRB on Dec 16, 2016 in Hartford, CT. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 16, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Hartford, CT (United States)

Additional Details

IRB