FDA inspection
IVWATCH, LLC: FDA inspection ending Aug 25, 2017
FDA inspection 1030070 · No Action Indicated (NAI) · Newport News, VA
Key facts
| Inspection ID | 1030070 |
|---|---|
| Firm | IVWATCH, LLC |
| FEI number | 3011490091 |
| Address | 700 Tech Center Parkway Ste 300 |
| City | Newport News |
| State | VA |
| ZIP | 23606 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Aug 25, 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