FDA inspection
Remel Europe Ltd.: FDA inspection ending Apr 4, 2019
FDA inspection 1116790 · Voluntary Action Indicated (VAI) · Dartford
Key facts
| Inspection ID | 1116790 |
|---|---|
| Firm | Remel Europe Ltd. |
| FEI number | 3003750284 |
| Address | Clipper Boulevard West |
| City | Dartford |
| Fiscal year | 2019 |
| Inspection end date | Apr 4, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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