FDA inspection
Redox S.r.l.: FDA inspection ending Feb 20, 2015
FDA inspection 917270 · Voluntary Action Indicated (VAI) · Monza
Key facts
| Inspection ID | 917270 |
|---|---|
| Firm | Redox S.r.l. |
| FEI number | 3006720740 |
| Address | Viale Gian Battista Stucchi 62/26 |
| City | Monza |
| Country | Italy |
| Fiscal year | 2015 |
| Inspection end date | Feb 20, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Unapproved and Misbranded Drugs |
| Product type | Drugs |
At a glance
- 1–9 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