FDA inspection
RANDOX LABORATORIES, LTD.: FDA inspection ending Apr 28, 2016
FDA inspection 969543 · Voluntary Action Indicated (VAI) · Crumlin
Key facts
| Inspection ID | 969543 |
|---|---|
| Firm | RANDOX LABORATORIES, LTD. |
| FEI number | 3006697287 |
| Address | 34 Diamond Rd |
| City | Crumlin |
| Country | United Kingdom |
| Fiscal year | 2016 |
| Inspection end date | Apr 28, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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