FDA inspection
Gyrus Medical Ltd.: FDA inspection ending Aug 5, 2010
FDA inspection 677234 · Official Action Indicated (OAI) · Cardiff
Key facts
| Inspection ID | 677234 |
|---|---|
| Firm | Gyrus Medical Ltd. |
| FEI number | 3002807134 |
| Address | Linea, Fortran Road |
| City | Cardiff |
| Country | United Kingdom |
| Fiscal year | 2010 |
| Inspection end date | Aug 5, 2010 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 144072 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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