FDA inspection
Astrea Fontaine: FDA inspection ending Jan 22, 2016
FDA inspection 957802 · Voluntary Action Indicated (VAI) · Fontaine Les Dijon
Key facts
| Inspection ID | 957802 |
|---|---|
| Firm | Astrea Fontaine |
| FEI number | 3002807473 |
| Address | Site de Fontaine, Rue Des Pres Potets |
| City | Fontaine Les Dijon |
| Country | France |
| Fiscal year | 2016 |
| Inspection end date | Jan 22, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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