FDA Inspection 1300422 — Nuvalent, Inc.

Nuvalent, Inc. — FEI 3017297026

The FDA completed an inspection of Nuvalent, Inc. on January 14, 2026 in Cambridge, MA. 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
January 14, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cambridge, MA (United States)

Additional Details

Sponsor, Contract Research Organization