FDA Inspection 921927 — Antoine Vonk Noordegraaf

Antoine Vonk Noordegraaf — FEI 3011353462

The FDA completed an inspection of Antoine Vonk Noordegraaf on April 17, 2015 in Amsterdam. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 17, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Amsterdam (Netherlands)

Additional Details

Clinical Investigator (CI)