FDA inspection
Covidien Ireland Limited: FDA inspection ending May 31, 2001
FDA inspection 75134 · No Action Indicated (NAI) · Tullamore
Key facts
| Inspection ID | 75134 |
|---|---|
| Firm | Covidien Ireland Limited |
| FEI number | 3002808143 |
| Address | Srah Road |
| City | Tullamore |
| Fiscal year | 2001 |
| Inspection end date | May 31, 2001 |
| 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