FDA inspection
Celerion Inc: FDA inspection ending Nov 21, 2019
FDA inspection 1114326 · No Action Indicated (NAI) · Lincoln, NE
Key facts
| Inspection ID | 1114326 |
|---|---|
| Firm | Celerion Inc |
| FEI number | 1915582 |
| Address | 621 Rose St |
| City | Lincoln |
| State | NE |
| ZIP | 68502 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Nov 21, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Bioresearch Monitoring |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data