FDA Inspection 719267 — Dr. Andre Vertruyen

Dr. Andre Vertruyen — FEI 3008802023

The FDA completed an inspection of Dr. Andre Vertruyen on April 7, 2011 in Antwerp. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 7, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Antwerp (Belgium)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
754521 CFR 312.120(c)Foreign clinical trials