FDA inspection
Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.): FDA inspection ending Dec 13, 2002
FDA inspection 251320 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 251320 |
|---|---|
| Firm | Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.) |
| FEI number | 2183620 |
| Address | 2575 University Ave W |
| City | Saint Paul |
| State | MN |
| ZIP | 55114-1073 |
| Fiscal year | 2003 |
| Inspection end date | Dec 13, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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