FDA inspection
Cordis Corporation: FDA inspection ending Nov 1, 2018
FDA inspection 1108598 · Voluntary Action Indicated (VAI) · Miami Lakes, FL
Key facts
| Inspection ID | 1108598 |
|---|---|
| Firm | Cordis Corporation |
| FEI number | 1016427 |
| Address | 14201 NW 60th Ave |
| City | Miami Lakes |
| State | FL |
| ZIP | 33014-2802 |
| Fiscal year | 2019 |
| Inspection end date | Nov 1, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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