FDA inspection
Eurofins Pharma Quality Control: FDA inspection ending Sep 8, 2017
FDA inspection 1091920 · Voluntary Action Indicated (VAI) · Les Ulis
Key facts
| Inspection ID | 1091920 |
|---|---|
| Firm | Eurofins Pharma Quality Control |
| FEI number | 3010164760 |
| Address | Laboratoire de Bromatologie de l, Lbe; ZAI de Courtaboeuf |
| City | Les Ulis |
| Country | France |
| Fiscal year | 2017 |
| Inspection end date | Sep 8, 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