FDA Inspection 1253475 — Lundbeck Pharmaceuticals LLC

Lundbeck Pharmaceuticals LLC — FEI 3004100593

The FDA completed an inspection of Lundbeck Pharmaceuticals LLC on Oct 25, 2024 in Deerfield, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 25, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Deerfield, IL (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)