FDA Inspection 652418 — Argus IRB Inc

Argus IRB Inc — FEI 3001452238

The FDA completed an inspection of Argus IRB Inc on Feb 24, 2010 in Tucson, AZ. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Tucson, AZ (United States)

Additional Details

IRB