FDA inspection
Eurofins Biopharma Product Testing Australia Pty. Ltd.: FDA inspection ending Mar 24, 2017
FDA inspection 1008506 · Voluntary Action Indicated (VAI) · Girraween
Key facts
| Inspection ID | 1008506 |
|---|---|
| Firm | Eurofins Biopharma Product Testing Australia Pty. Ltd. |
| FEI number | 3006635869 |
| Address | 8 Rachael CL |
| City | Girraween |
| Country | Australia |
| Fiscal year | 2017 |
| Inspection end date | Mar 24, 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