FDA Inspection 1307866 — Kumaran Deiva, MD, PhD

Kumaran Deiva, MD, PhD — FEI 3042129518

The FDA completed an inspection of Kumaran Deiva, MD, PhD on Feb 27, 2026 in Le Kremlin-Bicetre. 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
Feb 27, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Le Kremlin-Bicetre (France)

Additional details

Clinical Investigator (CI)

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