FDA Inspection
EidosmedEidosmed – FDA Inspection, Oct 21, 2010
Record Details
This FDA Inspection record concerns Eidosmed, with an inspection on October 21, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Eidosmed
- Inspection Date
- October 21, 2010
- Product Type
- Devices
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ID · 65df02c2-25a0-4421-ad6b-0622616295b9
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 695884
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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