FDA inspection
Evonik Rexim S.A.S.: FDA inspection ending Sep 6, 2019
FDA inspection 1105851 · No Action Indicated (NAI) · Ham
Key facts
| Inspection ID | 1105851 |
|---|---|
| Firm | Evonik Rexim S.A.S. |
| FEI number | 3002807994 |
| Address | Usine de Ham, 33 rue de Verdun |
| City | Ham |
| Country | France |
| Fiscal year | 2019 |
| Inspection end date | Sep 6, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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