FDA inspection
Regeneron Ireland Designated Activity Company: FDA inspection ending Sep 27, 2019
FDA inspection 1117521 · Voluntary Action Indicated (VAI) · Limerick
Key facts
| Inspection ID | 1117521 |
|---|---|
| Firm | Regeneron Ireland Designated Activity Company |
| FEI number | 3011684330 |
| Address | Raheen Business Park |
| City | Limerick |
| Country | Ireland |
| Fiscal year | 2019 |
| Inspection end date | Sep 27, 2019 |
| 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