FDA inspection
ECTOSENSE NV: FDA inspection ending Aug 31, 2023
FDA inspection 1216778 · Voluntary Action Indicated (VAI) · Rotselaar
Key facts
| Inspection ID | 1216778 |
|---|---|
| Firm | ECTOSENSE NV |
| FEI number | 3015548442 |
| Address | Bosbessenlaan 19a |
| City | Rotselaar |
| Country | Belgium |
| Fiscal year | 2023 |
| Inspection end date | Aug 31, 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