FDA inspection
Digitimer Ltd.: FDA inspection ending Jul 2, 2015
FDA inspection 934935 · Official Action Indicated (OAI) · Welwyn Garden City
Key facts
| Inspection ID | 934935 |
|---|---|
| Firm | Digitimer Ltd. |
| FEI number | 3003631667 |
| Address | 37 Hyde Way |
| City | Welwyn Garden City |
| Country | United Kingdom |
| Fiscal year | 2015 |
| Inspection end date | Jul 2, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
| Warning letter | 479856 |
At a glance
- None 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