FDA inspection
Cerner Corp: FDA inspection ending Sep 18, 2018
FDA inspection 1122961 · No Action Indicated (NAI) · Kansas City, MO
Key facts
| Inspection ID | 1122961 |
|---|---|
| Firm | Cerner Corp |
| FEI number | 1931259 |
| Address | 2800 Rock Creek Pkwy |
| City | Kansas City |
| State | MO |
| ZIP | 64117-2521 |
| Fiscal year | 2018 |
| Inspection end date | Sep 18, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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