FDA inspection
Fluke Electronics Corporation (Fluke Biomedical Inc.): FDA inspection ending Nov 10, 2003
FDA inspection 302637 · Voluntary Action Indicated (VAI) · Everett, WA
Key facts
| Inspection ID | 302637 |
|---|---|
| Firm | Fluke Electronics Corporation (Fluke Biomedical Inc.) |
| FEI number | 2921581 |
| Address | 6920 Seaway Blvd |
| City | Everett |
| State | WA |
| ZIP | 98203-5829 |
| Fiscal year | 2004 |
| Inspection end date | Nov 10, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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