FDA inspection
Remeda AB: FDA inspection ending Sep 14, 2023
FDA inspection 1220148 · Voluntary Action Indicated (VAI) · Halmstad
Key facts
| Inspection ID | 1220148 |
|---|---|
| Firm | Remeda AB |
| FEI number | 3013300766 |
| Address | Transportvagen 8 |
| City | Halmstad |
| Country | Sweden |
| Fiscal year | 2023 |
| Inspection end date | Sep 14, 2023 |
| 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