FDA inspection
Invivo Corporation: FDA inspection ending Oct 14, 2009
FDA inspection 622929 · Voluntary Action Indicated (VAI) · Orlando, FL
Key facts
| Inspection ID | 622929 |
|---|---|
| Firm | Invivo Corporation |
| FEI number | 1051786 |
| Address | 12151 Research Pkwy Ste 200 |
| City | Orlando |
| State | FL |
| ZIP | 32826 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Oct 14, 2009 |
| 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
- 10–99 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