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FDA Inspection 1057304 — Regeneron Pharmaceuticals Inc

Regeneron Pharmaceuticals Inc — FEI 1000521995

The FDA completed an inspection of Regeneron Pharmaceuticals Inc on June 18, 2018 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
June 18, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Tarrytown, NY (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

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FDA data resources