FDA Inspection 1068761 — Regeneron Pharmaceuticals Inc

Regeneron Pharmaceuticals Inc — FEI 1000521995

The FDA completed an inspection of Regeneron Pharmaceuticals Inc on September 17, 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
September 17, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tarrytown, NY (United States)