# FDA Inspection 988221 - Coeur Inc. - July 28, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/coeur-inc/0a259ce2-4f48-40f3-8dd2-8e3bb67885f2
Source feed: FDA_Inspections

> FDA Inspection 988221 for Coeur Inc. on July 28, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988221
- Company Name: Coeur Inc.
- Inspection Date: 2016-07-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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