# FDA Inspection 929470 - Eizo Corporation - April 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/eizo-corporation/c7f8db09-7dff-4007-bbe6-7175675de417
Source feed: FDA_Inspections

> FDA Inspection 929470 for Eizo Corporation on April 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 929470
- Company Name: Eizo Corporation
- Inspection Date: 2015-04-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 929470 - 2015-04-23](https://www.keypedia.com/records/fda_inspections/eizo-corporation/ec6aa794-1f37-49ba-8e37-0ad113f12054)
- [FDA Inspection 786439 - 2012-05-17](https://www.keypedia.com/records/fda_inspections/eizo-corporation/ce0d1d05-2c44-4f11-84b3-b719e7362b97)
- [FDA Inspection 786439 - 2012-05-17](https://www.keypedia.com/records/fda_inspections/eizo-corporation/eb3a2738-1db1-49fb-b6b8-3ecd313424ae)

Company: https://www.keypedia.com/companies/eizo-corporation/ebe10110-9bc6-47d0-b13a-17a1bd4edf76

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