# FDA Inspection 1302376 - Coeur Inc. - February 11, 2026

Source: https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/b3df6a8f-a77e-432e-9fad-695ef8d8eae5
Source feed: FDA_Inspections

> FDA Inspection 1302376 for Coeur Inc. on February 11, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1302376
- Company Name: Coeur Inc.
- Inspection Date: 2026-02-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1302376 - 2026-02-11](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/45765c8e-2475-4474-9c82-81b2fd33f057)
- [FDA Inspection 1302376 - 2026-02-11](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/c9860ad5-267f-4c1c-8fb8-a229da00bea5)
- [FDA Inspection 1302376 - 2026-02-11](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/cd210e86-bca8-45fd-b5a0-83024e06a07e)
- [FDA Inspection 1047741 - 2018-03-22](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/98b9abba-e0ba-4b59-a288-f7d1b2e2d48a)
- [FDA Inspection 988221 - 2016-07-28](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/06225c2b-1070-4aaa-87cf-d7ca5e5fdee7)

Company: https://www.globalkeysolutions.net/companies/coeur-inc/662d02ad-f9ca-4795-84e4-c95cc022e4f5

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