FDA inspection
Titertek Instruments Inc: FDA inspection ending Feb 10, 2015
FDA inspection 913796 · No Action Indicated (NAI) · Huntsville, AL
Key facts
| Inspection ID | 913796 |
|---|---|
| Firm | Titertek Instruments Inc |
| FEI number | 1028229 |
| Address | 5838 Research Park Blvd NW Ste 100 |
| City | Huntsville |
| State | AL |
| ZIP | 35806 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Feb 10, 2015 |
| 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