FDA inspection
Medtronic Bakken Research Center B.V.: FDA inspection ending Jul 29, 2016
FDA inspection 979523 · No Action Indicated (NAI) · Maastricht
Key facts
| Inspection ID | 979523 |
|---|---|
| Firm | Medtronic Bakken Research Center B.V. |
| FEI number | 3003276151 |
| Address | Endepolsdomein 5, 6229 GW Maastricht |
| City | Maastricht |
| Country | Netherlands |
| Fiscal year | 2016 |
| Inspection end date | Jul 29, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Bioresearch Monitoring |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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