FDA inspection
Dako North America Inc.: FDA inspection ending Oct 27, 2017
FDA inspection 1045809 · Voluntary Action Indicated (VAI) · Carpinteria, CA
Key facts
| Inspection ID | 1045809 |
|---|---|
| Firm | Dako North America Inc. |
| FEI number | 2022180 |
| Address | 1170 Mark Ave |
| City | Carpinteria |
| State | CA |
| ZIP | 93013-2918 |
| Fiscal year | 2018 |
| Inspection end date | Oct 27, 2017 |
| 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