# Eizo Corporation – FDA Inspection, May 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/eizo-corporation/eb3a2738-1db1-49fb-b6b8-3ecd313424ae
Source feed: FDA_Inspections

> FDA inspection 786439 of Eizo Corporation, May 17, 2012. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 786439
- Company Name: Eizo Corporation
- Inspection Date: 2012-05-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1044096 - 2017-08-03](https://www.keypedia.com/records/fda_inspections/eizo-corporation/9181c8eb-d41f-42c2-8761-a982a267c368)
- FDA Inspection 929470 - 2015-04-23

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