FDA inspection
Sebotek Hearing Systems, LLC: FDA inspection ending May 16, 2014
FDA inspection 881594 · No Action Indicated (NAI) · Tulsa, OK
Key facts
| Inspection ID | 881594 |
|---|---|
| Firm | Sebotek Hearing Systems, LLC |
| FEI number | 1643051 |
| Address | 2488 E 81st St Ste 2000 |
| City | Tulsa |
| State | OK |
| ZIP | 74137 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | May 16, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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