FDA inspection
Luminex Corporation: FDA inspection ending Mar 17, 2017
FDA inspection 1005213 · No Action Indicated (NAI) · Northbrook, IL
Key facts
| Inspection ID | 1005213 |
|---|---|
| Firm | Luminex Corporation |
| FEI number | 3006028115 |
| Address | 4088 Commercial Ave |
| City | Northbrook |
| State | IL |
| ZIP | 60062 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Mar 17, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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