FDA inspection
Celsion Corporation: FDA inspection ending Dec 18, 2003
FDA inspection 304381 · Official Action Indicated (OAI) · Columbia, MD
Key facts
| Inspection ID | 304381 |
|---|---|
| Firm | Celsion Corporation |
| FEI number | 1122126 |
| Address | 10220 Old Columbia Rd Ste L |
| City | Columbia |
| State | MD |
| ZIP | 21046-2391 |
| Fiscal year | 2004 |
| Inspection end date | Dec 18, 2003 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
| Warning letter | UCM146851 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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