FDA inspection
Hikma Farmaceutica, (Portugal) S.A.: FDA inspection ending Apr 12, 2016
FDA inspection 970483 · Voluntary Action Indicated (VAI) · Terrugem Snt
Key facts
| Inspection ID | 970483 |
|---|---|
| Firm | Hikma Farmaceutica, (Portugal) S.A. |
| FEI number | 3002807173 |
| Address | Estrada Do Rio Da Mo |
| City | Terrugem Snt |
| Country | Portugal |
| Fiscal year | 2016 |
| Inspection end date | Apr 12, 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
- No Establishment inspection report (EIR) exists
- 10–99 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