FDA inspection
CareFusion 303, Inc.: FDA inspection ending Dec 18, 2012
FDA inspection 812020 · Official Action Indicated (OAI) · San Diego, CA
Key facts
| Inspection ID | 812020 |
|---|---|
| Firm | CareFusion 303, Inc. |
| FEI number | 2016493 |
| Address | 10020 Pacific Mesa Blvd |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Dec 18, 2012 |
| Classification | Official Action Indicated (OAI) |
| 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
- 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