FDA inspection
Croda Europe Ltd.: FDA inspection ending Sep 16, 2016
FDA inspection 990109 · Voluntary Action Indicated (VAI) · Widnes
Key facts
| Inspection ID | 990109 |
|---|---|
| Firm | Croda Europe Ltd. |
| FEI number | 3004214492 |
| Address | Foundry Lane |
| City | Widnes |
| Country | United Kingdom |
| Fiscal year | 2016 |
| Inspection end date | Sep 16, 2016 |
| 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