FDA inspection
Lumitex Medical Devices Inc: FDA inspection ending Dec 26, 2013
FDA inspection 859893 · No Action Indicated (NAI) · Brecksville, OH
Key facts
| Inspection ID | 859893 |
|---|---|
| Firm | Lumitex Medical Devices Inc |
| FEI number | 1000122810 |
| Address | 8300 Dow Cir |
| City | Brecksville |
| State | OH |
| ZIP | 44141 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Dec 26, 2013 |
| 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