FDA inspection
Neurolumen LLC: FDA inspection ending Dec 13, 2013
FDA inspection 859558 · Official Action Indicated (OAI) · Oklahoma City, OK
Key facts
| Inspection ID | 859558 |
|---|---|
| Firm | Neurolumen LLC |
| FEI number | 3010144038 |
| Address | 9636 N May Ave Ste 230 |
| City | Oklahoma City |
| State | OK |
| ZIP | 73120 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Dec 13, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 422220 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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