FDA inspection
Catalent U.K. Swindon Zydis Limited: FDA inspection ending Jul 26, 2018
FDA inspection 1064287 · Voluntary Action Indicated (VAI) · Swindon
Key facts
| Inspection ID | 1064287 |
|---|---|
| Firm | Catalent U.K. Swindon Zydis Limited |
| FEI number | 3003812585 |
| Address | Frankland Road, Swd |
| City | Swindon |
| Country | United Kingdom |
| Fiscal year | 2018 |
| Inspection end date | Jul 26, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Vaccines and Allergenic Products |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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