FDA inspection
Lucideon Limited: FDA inspection ending Sep 10, 2019
FDA inspection 1101554 · Voluntary Action Indicated (VAI) · Stoke-On-Trent
Key facts
| Inspection ID | 1101554 |
|---|---|
| Firm | Lucideon Limited |
| FEI number | 3001231132 |
| Address | Penkhull, Queens Road |
| City | Stoke-On-Trent |
| Fiscal year | 2019 |
| Inspection end date | Sep 10, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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