FDA Inspection 1337300 — Jeanine Roodhart, M.D., Ph.D.

Jeanine Roodhart, M.D., Ph.D. — FEI 3046963646

The FDA completed an inspection of Jeanine Roodhart, M.D., Ph.D. on Sep 17, 2026 in Utrecht. 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
Sep 17, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Utrecht (Netherlands)

Additional Details

Clinical Investigator (CI)

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