FDA Inspection 1122441 — Allendale Investigational Review Board

Allendale Investigational Review Board — FEI 1000526912

The FDA completed an inspection of Allendale Investigational Review Board on March 19, 2020 in Old Lyme, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 19, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Old Lyme, CT (United States)

Additional Details

IRB