FDA inspection
Codan US Corporation: FDA inspection ending Jul 20, 2018
FDA inspection 1059719 · Voluntary Action Indicated (VAI) · Santa Ana, CA
Key facts
| Inspection ID | 1059719 |
|---|---|
| Firm | Codan US Corporation |
| FEI number | 2016945 |
| Address | 3501 W Sunflower Ave |
| City | Santa Ana |
| State | CA |
| ZIP | 92704 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jul 20, 2018 |
| 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