FDA Inspection 1043415 — Greenwich Hospital IRB

Greenwich Hospital IRB — FEI 1219116

The FDA completed an inspection of Greenwich Hospital IRB on Jan 12, 2018 in Greenwich, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 12, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Greenwich, CT (United States)

Additional Details

IRB