FDA Inspection 725652 — Alejandro Rodolfo, MD

Alejandro Rodolfo, MD — FEI 3007374238

The FDA completed an inspection of Alejandro Rodolfo, MD on May 10, 2011 in Miami, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 10, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Sponsor, Contract Research Organization