FDA inspection
Hovione Limited: FDA inspection ending May 20, 2016
FDA inspection 973523 · Voluntary Action Indicated (VAI) · Cork
Key facts
| Inspection ID | 973523 |
|---|---|
| Firm | Hovione Limited |
| FEI number | 3008058822 |
| Address | Loughbeg Drug Product Plant |
| City | Cork |
| Fiscal year | 2016 |
| Inspection end date | May 20, 2016 |
| 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