FDA inspection
Eurofins Viracor, LLC.: FDA inspection ending Jul 26, 2019
FDA inspection 1097599 · Voluntary Action Indicated (VAI) · Lenexa, KS
Key facts
| Inspection ID | 1097599 |
|---|---|
| Firm | Eurofins Viracor, LLC. |
| FEI number | 3005651716 |
| Address | 951 Nw Technology Dr |
| City | Lenexa |
| State | KS |
| ZIP | 66219 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jul 26, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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