# FDA Inspection 840625 - Medtronic Sofamor Danek USA, Inc - July 15, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-sofamor-danek-usa-inc/1275661e-9a39-4f80-a9b7-dcd2943249a3
Source feed: FDA_Inspections

> FDA Inspection 840625 for Medtronic Sofamor Danek USA, Inc on July 15, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840625
- Company Name: Medtronic Sofamor Danek USA, Inc
- Inspection Date: 2013-07-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- 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/1803c0d5-74d1-4e22-9d2a-65ddba605290

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