# FDA 483 - Medtronic Neuromodulation - January 21, 2011

Source: https://www.globalkeysolutions.net/records/483/medtronic-neuromodulation/f21b8cb5-3478-4780-aec4-4e5833994a7e

> FDA 483 for Medtronic Neuromodulation on January 21, 2011. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Medtronic Neuromodulation
- Inspection Date: 2011-01-21
- Product Type: device
- Office Name: Minneapolis District Office

## Related Officers

- [Susan M. Atcher](https://www.globalkeysolutions.net/people/susan-m-atcher/445bf2f8-3a11-4e9b-8663-87a42b2e8757)
- [Jessica L. Johnson](https://www.globalkeysolutions.net/people/jessica-l-johnson/9ea42c42-c28b-4945-a862-6b77617177f9)

Company: https://www.globalkeysolutions.net/companies/medtronic-neuromodulation/8379de30-31d7-45f5-a6e2-7f541f95e6f5

Office: https://www.globalkeysolutions.net/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d