FDA inspection
Kaneka Eurogentec SA: FDA inspection ending Oct 27, 2017
FDA inspection 1037724 · Voluntary Action Indicated (VAI) · Seraing
Key facts
| Inspection ID | 1037724 |
|---|---|
| Firm | Kaneka Eurogentec SA |
| FEI number | 3003323169 |
| Address | Rue du Bois Saint-Jean 14 |
| City | Seraing |
| Country | Belgium |
| Fiscal year | 2018 |
| Inspection end date | Oct 27, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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