FDA Inspection 1261246 — Celerion Inc

Celerion Inc — FEI 1915582

The FDA completed an inspection of Celerion Inc on January 17, 2025 in Lincoln, NE. 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 17, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lincoln, NE (United States)

Additional Details

Bioanalytical BA/BE