FDA Inspection 1301040 — Regeneron Pharmaceuticals, Inc.
The FDA completed an inspection of Regeneron Pharmaceuticals, Inc. on March 27, 2026 in Armonk, 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
- March 27, 2026
- Fiscal Year
- 2026
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Armonk, NY (United States)
Additional Details
Sponsor, Contract Research Organization