FDA Inspection 1275656 — Newark Beth Israel Med Ctr IRB

Newark Beth Israel Med Ctr IRB — FEI 2243240

The FDA completed an inspection of Newark Beth Israel Med Ctr IRB on July 2, 2025 in Newark, NJ. 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
July 2, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newark, NJ (United States)

Additional Details

IRB