FDA inspection
Eldon Biologicals A/S: FDA inspection ending Aug 27, 2003
FDA inspection 291767 · Official Action Indicated (OAI) · Gentofte
Key facts
| Inspection ID | 291767 |
|---|---|
| Firm | Eldon Biologicals A/S |
| FEI number | 3003783142 |
| Address | Sandtoften 10 |
| City | Gentofte |
| Fiscal year | 2003 |
| Inspection end date | Aug 27, 2003 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM147927 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- Yes 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