FDA Inspection 1269430 — Biohaven Pharmaceuticals, Inc

Biohaven Pharmaceuticals, Inc — FEI 3010802167

The FDA completed an inspection of Biohaven Pharmaceuticals, Inc on April 24, 2025 in New Haven, CT. 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
April 24, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
New Haven, CT (United States)

Additional Details

Sponsor, Contract Research Organization