FDA Inspection 1041891 — Geert D'Haens

Geert D'Haens — FEI 3013665123

The FDA completed an inspection of Geert D'Haens on Oct 27, 2017 in Amsterdam. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 27, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Amsterdam (Netherlands)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.