# FDA Inspection 572942 - Coeur Inc. - April 01, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/4f202aa3-3e56-4506-a516-7feaa484b63f
Source feed: FDA_Inspections

> FDA Inspection 572942 for Coeur Inc. on April 01, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 572942
- Company Name: Coeur Inc.
- Inspection Date: 2009-04-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: 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 1302376 - 2026-02-11](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/b3df6a8f-a77e-432e-9fad-695ef8d8eae5)
- [FDA Inspection 1047741 - 2018-03-22](https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/98b9abba-e0ba-4b59-a288-f7d1b2e2d48a)

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
