FDA inspection
Dilon Technologies France SAS: FDA inspection ending Oct 29, 2015
FDA inspection 949043 · Voluntary Action Indicated (VAI) · Saint-Priest
Key facts
| Inspection ID | 949043 |
|---|---|
| Firm | Dilon Technologies France SAS |
| FEI number | 3007702492 |
| Address | Batiment 7, 8 allee Irene Joliot Curie |
| City | Saint-Priest |
| Country | France |
| Fiscal year | 2016 |
| Inspection end date | Oct 29, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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