FDA inspection
Proactive Medical Products, LLC: FDA inspection ending Dec 20, 2017
FDA inspection 1039068 · No Action Indicated (NAI) · Mount Vernon, NY
Key facts
| Inspection ID | 1039068 |
|---|---|
| Firm | Proactive Medical Products, LLC |
| FEI number | 3009327812 |
| Address | 270 Washington St |
| City | Mount Vernon |
| State | NY |
| ZIP | 10550 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Dec 20, 2017 |
| 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