# Medtronic MiniMed, Inc. – FDA Inspection, Mar 24, 2017

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

> FDA inspection 1005666 of Medtronic MiniMed, Inc., March 24, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 13 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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- [FDA Inspection 1199488 - 2023-03-10](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/8d4837ff-b122-4e9b-96ed-06ae9c86bb88)
- [FDA Inspection 1145642 - 2021-07-07](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/d6b25b74-2795-4765-834a-59933f9912cb)
- FDA Inspection 1082648 - 2019-02-15
- [FDA Inspection 1044249 - 2018-03-14](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/edacd75d-2a95-421f-9b12-b7a586c0639f)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

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