FDA Inspection
Coeur Inc.Coeur Inc. – FDA Inspection, Jul 28, 2016
Record Details
This FDA Inspection record concerns Coeur Inc., with an inspection on July 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Coeur Inc.
- Inspection Date
- July 28, 2016
- Product Type
- Devices
View Company Profile
ID · 0a259ce2-4f48-40f3-8dd2-8e3bb67885f2
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 988221
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Coeur Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 11, 2026 | NAI | Atlanta District Office | Postmarket Assurance: Medical Devices |
| March 22, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 23, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 1, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Coeur Inc.
- FDA Inspection 1302376 - 2026-02-11
- FDA Inspection 1047741 - 2018-03-22
- FDA Inspection 795827 - 2012-08-23
- FDA Inspection 572942 - 2009-04-01
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