# FDA Inspection 695884 - Eidosmed - October 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/eidosmed/41501e00-fbf8-4490-966d-4ff9a9fb8200
Source feed: FDA_Inspections

> FDA Inspection 695884 for Eidosmed on October 21, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695884
- Company Name: Eidosmed
- Inspection Date: 2010-10-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 695884 - 2010-10-21](https://www.keypedia.com/records/fda_inspections/eidosmed/65df02c2-25a0-4421-ad6b-0622616295b9)

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