FDA Inspection 1019856 — Johan Vande Walle

Johan Vande Walle — FEI 3013552827

The FDA completed an inspection of Johan Vande Walle on Jul 4, 2017 in Gent. 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
Jul 4, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Gent (Belgium)

Additional details

Clinical Investigator (CI)

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