FDA Inspection 1038127 — Lundbeck Pharmaceuticals LLC

Lundbeck Pharmaceuticals LLC — FEI 3004100593

The FDA completed an inspection of Lundbeck Pharmaceuticals LLC on Nov 20, 2017 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
Nov 20, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Deerfield, IL (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)