FDA inspection
Neurotron Medical Inc.: FDA inspection ending Nov 23, 2015
FDA inspection 971930 · Voluntary Action Indicated (VAI) · Warminster, PA
Key facts
| Inspection ID | 971930 |
|---|---|
| Firm | Neurotron Medical Inc. |
| FEI number | 2245302 |
| Address | 800 Silvia St |
| City | Warminster |
| State | PA |
| ZIP | 18974 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Nov 23, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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