FDA inspection
Rinovum Subsidiary 2 LLC: FDA inspection ending May 11, 2017
FDA inspection 1019524 · No Action Indicated (NAI) · Export, PA
Key facts
| Inspection ID | 1019524 |
|---|---|
| Firm | Rinovum Subsidiary 2 LLC |
| FEI number | 3015417614 |
| Address | 300 Oxford Dr Ste 330 |
| City | Export |
| State | PA |
| ZIP | 15632 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | May 11, 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