FDA inspection
Hovione Limited: FDA inspection ending Dec 22, 2017
FDA inspection 1041771 · No Action Indicated (NAI) · Ringaskiddy
Key facts
| Inspection ID | 1041771 |
|---|---|
| Firm | Hovione Limited |
| FEI number | 3008058822 |
| Address | Loughbeg Drug Product Plant |
| City | Ringaskiddy |
| Country | Ireland |
| Fiscal year | 2018 |
| Inspection end date | Dec 22, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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