# FDA Inspection 1022946 - Medtronic MiniMed, Inc. - August 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/112e4d99-79c8-4e9e-9c58-e9fbb0ad0052
Source feed: FDA_Inspections

> FDA Inspection 1022946 for Medtronic MiniMed, Inc. on August 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022946
- Company Name: Medtronic MiniMed, Inc.
- Inspection Date: 2017-08-14
- 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.keypedia.com/companies/medtronic-minimed-inc/a75f6a75-6d10-41f1-8c92-839535f005bf

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