FDA inspection
Arrotek Medical Ltd: FDA inspection ending Jul 30, 2015
FDA inspection 940228 · Voluntary Action Indicated (VAI) · Sligo
Key facts
| Inspection ID | 940228 |
|---|---|
| Firm | Arrotek Medical Ltd |
| FEI number | 3005255160 |
| Address | Dublin Road Business Park |
| City | Sligo |
| Country | Ireland |
| Fiscal year | 2015 |
| Inspection end date | Jul 30, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 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