FDA inspection
Cambridge Diagnostic Products, Inc.: FDA inspection ending Jan 10, 2013
FDA inspection 816931 · Voluntary Action Indicated (VAI) · Ft Lauderdale, FL
Key facts
| Inspection ID | 816931 |
|---|---|
| Firm | Cambridge Diagnostic Products, Inc. |
| FEI number | 1029182 |
| Address | 6880 NW 17th Ave |
| City | Ft Lauderdale |
| State | FL |
| ZIP | 33309 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jan 10, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
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
- 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