FDA inspection
Medtronic MiniMed, Inc.: FDA inspection ending Dec 16, 2013
FDA inspection 859043 · Voluntary Action Indicated (VAI) · Northridge, CA
Key facts
| Inspection ID | 859043 |
|---|---|
| Firm | Medtronic MiniMed, Inc. |
| FEI number | 3003166194 |
| Address | 18000 Devonshire St |
| City | Northridge |
| State | CA |
| ZIP | 91325 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Dec 16, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| Product type | Devices |
| Warning letter | 405884 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- Yes 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