FDA Inspection 625470 — Ochsner Clinic Foundation IRB

Ochsner Clinic Foundation IRB — FEI 2310313

The FDA completed an inspection of Ochsner Clinic Foundation IRB on Oct 20, 2009 in New Orleans, LA. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 20, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New Orleans, LA (United States)

Additional Details

IRB