FDA Inspection 1272587 — Virtua Health IRB

Virtua Health IRB — FEI 3007160443

The FDA completed an inspection of Virtua Health IRB on June 6, 2025 in Marlton, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 6, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Marlton, NJ (United States)

Additional Details

IRB