FDA Inspection 1232732 — Regeneron Pharmaceuticals Inc

Regeneron Pharmaceuticals Inc — FEI 1000521995

The FDA completed an inspection of Regeneron Pharmaceuticals Inc on May 1, 2024 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
May 1, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Tarrytown, NY (United States)

Additional Details

Sponsor, Contract Research Organization