FDA inspection
Regeneron Ireland Designated Activity Company: FDA inspection ending Dec 5, 2017
FDA inspection 1034098 · Voluntary Action Indicated (VAI) · Limerick
Key facts
| Inspection ID | 1034098 |
|---|---|
| Firm | Regeneron Ireland Designated Activity Company |
| FEI number | 3011684330 |
| Address | Raheen Business Park |
| City | Limerick |
| Fiscal year | 2018 |
| Inspection end date | Dec 5, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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