FDA Inspection 1292476 — Regeneron Pharmaceuticals Inc

Regeneron Pharmaceuticals Inc — FEI 1000521995

The FDA completed an inspection of Regeneron Pharmaceuticals Inc on December 10, 2025 in Tarrytown, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 10, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Tarrytown, NY (United States)

Additional Details

Bioanalytical BA/BE