FDA inspection
FUJIFILM Diosynth Biotechnologies UK Limited: FDA inspection ending Jul 11, 2014
FDA inspection 894612 · Voluntary Action Indicated (VAI) · Billingham
Key facts
| Inspection ID | 894612 |
|---|---|
| Firm | FUJIFILM Diosynth Biotechnologies UK Limited |
| FEI number | 3007182567 |
| Address | Belasis Avenue |
| City | Billingham |
| Country | United Kingdom |
| Fiscal year | 2014 |
| Inspection end date | Jul 11, 2014 |
| 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