# FDA Inspection 950920 - Medtronic Sofamor Danek USA Inc - November 03, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-sofamor-danek-usa-inc/1c51cc6b-5494-456d-9390-47a1e6f87905
Source feed: FDA_Inspections

> FDA Inspection 950920 for Medtronic Sofamor Danek USA Inc on November 03, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950920
- Company Name: Medtronic Sofamor Danek USA Inc
- Inspection Date: 2015-11-03
- 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-sofamor-danek-usa-inc/335e1ae6-cdf4-4132-81da-e8914c45ec7c

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