FDA inspection
Alexander Technologies Europe LTD.: FDA inspection ending May 14, 2003
FDA inspection 273012 · Voluntary Action Indicated (VAI) · Mason City, IA
Key facts
| Inspection ID | 273012 |
|---|---|
| Firm | Alexander Technologies Europe LTD. |
| FEI number | 1928225 |
| Address | 1511 S Garfield Pl, Box 1508 |
| City | Mason City |
| State | IA |
| ZIP | 50401-5662 |
| Fiscal year | 2003 |
| Inspection end date | May 14, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No 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