FDA inspection
Versiti Michigan, Inc: FDA inspection ending Jan 15, 2009
FDA inspection 558852 · No Action Indicated (NAI) · Traverse City, MI
Key facts
| Inspection ID | 558852 |
|---|---|
| Firm | Versiti Michigan, Inc |
| FEI number | 1000517886 |
| Address | 2575 Aero Park Dr |
| City | Traverse City |
| State | MI |
| ZIP | 49686 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jan 15, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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