# FDA Inspection 859943 - Medtronic Neuromodulation - December 19, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-neuromodulation/fcf09381-95d0-4028-9e75-3f50f76d4ffb/
Source feed: FDA_Inspections

> FDA Inspection 859943 for Medtronic Neuromodulation on December 19, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 859943
- Company Name: Medtronic Neuromodulation
- Inspection Date: 2013-12-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/medtronic-neuromodulation/2a0b2563-ee1c-4a97-a37a-e714223e0f65

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7