FDA inspection
Celerion Inc: FDA inspection ending Feb 1, 2008
FDA inspection 507634 · No Action Indicated (NAI) · Lincoln, NE
Key facts
| Inspection ID | 507634 |
|---|---|
| Firm | Celerion Inc |
| FEI number | 1915582 |
| Address | 621 Rose St |
| City | Lincoln |
| State | NE |
| ZIP | 68502-2040 |
| Fiscal year | 2008 |
| Inspection end date | Feb 1, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Bio-Research Monit: Human Drugs |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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