FDA inspection
MELOQ AB: FDA inspection ending Mar 9, 2023
FDA inspection 1199271 · Voluntary Action Indicated (VAI) · Stockholm
Key facts
| Inspection ID | 1199271 |
|---|---|
| Firm | MELOQ AB |
| FEI number | 3013687630 |
| Address | Drakenbergsgatan 9 |
| City | Stockholm |
| Country | Sweden |
| Fiscal year | 2023 |
| Inspection end date | Mar 9, 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