# FDA Inspection 1066467 - Eizo GmbH - September 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/eizo-gmbh/837456b9-6229-4928-827e-e95b9d2d069e
Source feed: FDA_Inspections

> FDA Inspection 1066467 for Eizo GmbH on September 20, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066467
- Company Name: Eizo GmbH
- Inspection Date: 2018-09-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/eizo-gmbh/5bb23070-4c01-4ed1-96f4-adcc8962f72b

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