FDA inspection
Gambro UF Solutions, Inc.: FDA inspection ending May 13, 2003
FDA inspection 274818 · Voluntary Action Indicated (VAI) · Minneapolis, MN
Key facts
| Inspection ID | 274818 |
|---|---|
| Firm | Gambro UF Solutions, Inc. |
| FEI number | 3003504604 |
| Address | 7601 Northland Dr N Ste 170 |
| City | Minneapolis |
| State | MN |
| ZIP | 55428-4529 |
| Fiscal year | 2003 |
| Inspection end date | May 13, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None 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