FDA inspection
Vitalograph (Ireland), Ltd.: FDA inspection ending May 22, 2008
FDA inspection 522975 · No Action Indicated (NAI) · Ennis
Key facts
| Inspection ID | 522975 |
|---|---|
| Firm | Vitalograph (Ireland), Ltd. |
| FEI number | 3002808458 |
| Address | Gort Road Business Park |
| City | Ennis |
| Fiscal year | 2008 |
| Inspection end date | May 22, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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