FDA Inspection 1114326 — Celerion Inc

Celerion Inc — FEI 1915582

The FDA completed an inspection of Celerion Inc on November 21, 2019 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
November 21, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lincoln, NE (United States)

Additional Details

Clinical BA/BE