# FDA Inspection 1223359 - Senseonics, Inc. - November 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/senseonics-inc/ecd86414-e087-4cc9-9dfb-d83141c41aef
Source feed: FDA_Inspections

> FDA Inspection 1223359 for Senseonics, Inc. on November 17, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1223359
- Company Name: Senseonics, Inc.
- Inspection Date: 2023-11-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1223359 - 2023-11-17](https://www.keypedia.com/records/fda_inspections/senseonics-inc/244307bf-f852-4f8c-bde1-53d95f14b415)
- [FDA Inspection 1006694 - 2017-04-04](https://www.keypedia.com/records/fda_inspections/senseonics-inc/4c073cfc-8db3-4ac9-bdba-de5f38f7bd0b)
- [FDA Inspection 999591 - 2017-01-31](https://www.keypedia.com/records/fda_inspections/senseonics-inc/d0212bb6-4a72-4e6d-a977-7c6cc47fbda6)

Company: https://www.keypedia.com/companies/senseonics-inc/d243cecd-6ebe-47f7-904b-5a8c324f1460

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