FDA inspection
Astellas Ireland Co Ltd: FDA inspection ending Mar 8, 2013
FDA inspection 823111 · Voluntary Action Indicated (VAI) · Killorglin
Key facts
| Inspection ID | 823111 |
|---|---|
| Firm | Astellas Ireland Co Ltd |
| FEI number | 3002807020 |
| Address | Bansha |
| City | Killorglin |
| Country | Ireland |
| Fiscal year | 2013 |
| Inspection end date | Mar 8, 2013 |
| 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