FDA inspection
Medtronic Xomed, Inc.: FDA inspection ending Aug 16, 2005
FDA inspection 390880 · No Action Indicated (NAI) · Mystic, CT
Key facts
| Inspection ID | 390880 |
|---|---|
| Firm | Medtronic Xomed, Inc. |
| FEI number | 1000159144 |
| Address | 950 Flanders Rd |
| City | Mystic |
| State | CT |
| ZIP | 06355-1314 |
| Fiscal year | 2005 |
| Inspection end date | Aug 16, 2005 |
| 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
- 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