FDA Inspection 1003940 — Stefan Bourgeois, M.D.

Stefan Bourgeois, M.D. — FEI 3013186125

The FDA completed an inspection of Stefan Bourgeois, M.D. on Mar 1, 2017 in Antwerp. 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
Mar 1, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Antwerp (Belgium)

Additional Details

Clinical Investigator (CI)

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