FDA inspection
EBIS Iotron Ltd.: FDA inspection ending Jul 11, 2002
FDA inspection 237679 · Voluntary Action Indicated (VAI) · Didcot Oxon
Key facts
| Inspection ID | 237679 |
|---|---|
| Firm | EBIS Iotron Ltd. |
| FEI number | 3000262694 |
| Address | 418 Harwell |
| City | Didcot Oxon |
| Fiscal year | 2002 |
| Inspection end date | Jul 11, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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