FDA inspection
Cambridge Diagnostic Products, Inc.: FDA inspection ending Mar 16, 2023
FDA inspection 1201734 · Voluntary Action Indicated (VAI) · Ft Lauderdale, FL
Key facts
| Inspection ID | 1201734 |
|---|---|
| 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 | 2023 |
| Inspection end date | Mar 16, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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