# Eidosmed – FDA Inspection, Oct 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/eidosmed/65df02c2-25a0-4421-ad6b-0622616295b9
Source feed: FDA_Inspections

> FDA inspection 695884 of Eidosmed, October 21, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695884
- Company Name: Eidosmed
- Inspection Date: 2010-10-21
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

Company: https://www.keypedia.com/companies/eidosmed/6b9a337b-51bf-494c-9356-be56380b4d74

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