FDA inspection
ImpactLife: FDA inspection ending Jun 25, 2014
FDA inspection 885325 · Voluntary Action Indicated (VAI) · Davenport, IA
Key facts
| Inspection ID | 885325 |
|---|---|
| Firm | ImpactLife |
| FEI number | 1970356 |
| Address | 5500 Lakeview Pkwy |
| City | Davenport |
| State | IA |
| ZIP | 52807 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Jun 25, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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