# FDA Inspection 1005666 - Medtronic MiniMed, Inc. - March 24, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-minimed-inc/fa6d117d-ca0a-4b8c-af3e-742354fb7592/
Source feed: FDA_Inspections

> FDA Inspection 1005666 for Medtronic MiniMed, Inc. on March 24, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005666
- Company Name: Medtronic MiniMed, Inc.
- Inspection Date: 2017-03-24
- 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-minimed-inc/a75f6a75-6d10-41f1-8c92-839535f005bf

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