FDA inspection
Invia, Llc: FDA inspection ending Jan 15, 2010
FDA inspection 645542 · Voluntary Action Indicated (VAI) · Ann Arbor, MI
Key facts
| Inspection ID | 645542 |
|---|---|
| Firm | Invia, Llc |
| FEI number | 3004993756 |
| Address | 3025 Boardwalk St Ste 200 |
| City | Ann Arbor |
| State | MI |
| ZIP | 48108 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Jan 15, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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