FDA inspection
Eisai Manufacturing Limited: FDA inspection ending May 13, 2016
FDA inspection 974401 · Voluntary Action Indicated (VAI) · Hatfield
Key facts
| Inspection ID | 974401 |
|---|---|
| Firm | Eisai Manufacturing Limited |
| FEI number | 3008356774 |
| Address | European Knowledge Centre, Mosquito Way |
| City | Hatfield |
| Country | United Kingdom |
| Fiscal year | 2016 |
| Inspection end date | May 13, 2016 |
| 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