FDA inspection
Eurofarma Laboratorios S.A.: FDA inspection ending Sep 20, 2022
FDA inspection 1180012 · Voluntary Action Indicated (VAI) · Itapevi
Key facts
| Inspection ID | 1180012 |
|---|---|
| Firm | Eurofarma Laboratorios S.A. |
| FEI number | 3009538725 |
| Address | Rodovia Presidente Castelo Branco, 3565, Quadragl Lote A |
| City | Itapevi |
| Country | Brazil |
| Fiscal year | 2022 |
| Inspection end date | Sep 20, 2022 |
| 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
- 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