# Coeur Inc. – FDA Inspection, Mar 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/coeur-inc/98b9abba-e0ba-4b59-a288-f7d1b2e2d48a
Source feed: FDA_Inspections

> FDA inspection 1047741 of Coeur Inc., March 22, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047741
- Company Name: Coeur Inc.
- Inspection Date: 2018-03-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1302376 - 2026-02-11](https://www.keypedia.com/records/fda_inspections/coeur-inc/45765c8e-2475-4474-9c82-81b2fd33f057)
- [FDA Inspection 988221 - 2016-07-28](https://www.keypedia.com/records/fda_inspections/coeur-inc/0a259ce2-4f48-40f3-8dd2-8e3bb67885f2)
- FDA Inspection 795827 - 2012-08-23
- FDA Inspection 572942 - 2009-04-01

## Related Officers

- [Monica C. Burgos Garcia](https://www.keypedia.com/people/monica-c-burgos-garcia/d73d6ad6-4158-4c12-a0bf-6f5721db3400)

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

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