FDA inspection
Zenith Diagnostics: FDA inspection ending Nov 20, 2018
FDA inspection 1072319 · Voluntary Action Indicated (VAI) · Arlington Heights, IL
Key facts
| Inspection ID | 1072319 |
|---|---|
| Firm | Zenith Diagnostics |
| FEI number | 3006493142 |
| Address | 1000 King George Post Rd Unit 3 |
| City | Arlington Heights |
| State | IL |
| ZIP | 60005 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Nov 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