FDA inspection
Amplivox Ltd: FDA inspection ending Dec 15, 2011
FDA inspection 761210 · Official Action Indicated (OAI) · Oxford
Key facts
| Inspection ID | 761210 |
|---|---|
| Firm | Amplivox Ltd |
| FEI number | 3003138182 |
| Address | 29-30 Station Field Est,Kidlington |
| City | Oxford |
| Country | United Kingdom |
| Fiscal year | 2012 |
| Inspection end date | Dec 15, 2011 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 290397 |
At a glance
- 10–99 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