FDA Warning Letter — Medtronic Neuromodulation
The FDA took a Warning Letter action against Medtronic Neuromodulation on Jul 17, 2012 (Minneapolis, MN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action details
- Facility
- Medtronic Neuromodulation
- Date
- Jul 17, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Center
- CDRH
- Location
- Minneapolis, MN (United States)