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FDA Inspection 1293396 — Animesh Rathore, MD

Animesh Rathore, MD — FEI 3040335419

The FDA completed an inspection of Animesh Rathore, MD on Nov 21, 2025 in Norfolk, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 21, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Norfolk, VA (United States)

Additional details

Clinical Investigator (CI)

Facility

FDA data resources

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