FDA inspection
Cogent Technology, Ltd.: FDA inspection ending Feb 14, 2019
FDA inspection 1079221 · Voluntary Action Indicated (VAI) · Woodbridge
Key facts
| Inspection ID | 1079221 |
|---|---|
| Firm | Cogent Technology, Ltd. |
| FEI number | 3002806730 |
| Address | Dock Lane |
| City | Woodbridge |
| Country | United Kingdom |
| Fiscal year | 2019 |
| Inspection end date | Feb 14, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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