FDA inspection
Quidel Corporation: FDA inspection ending Apr 10, 2017
FDA inspection 1010641 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 1010641 |
|---|---|
| Firm | Quidel Corporation |
| FEI number | 2024674 |
| Address | 10165 McKellar Ct |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Apr 10, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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
- 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