# FDA Inspection 1016443 - Medtronic Neuromodulation - June 30, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-neuromodulation/dc924c14-2eef-491d-a294-73fc7826b1b6
Source feed: FDA_Inspections

> FDA Inspection 1016443 for Medtronic Neuromodulation on June 30, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016443
- Company Name: Medtronic Neuromodulation
- Inspection Date: 2017-06-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- 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