# Eizo GmbH – FDA Inspection, Mar 28, 2012

Source: https://www.keypedia.com/records/fda_inspections/eizo-gmbh/b3b048ed-28f0-401a-8515-040eb1dde590
Source feed: FDA_Inspections

> FDA inspection 779687 of Eizo GmbH, March 28, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 779687
- Company Name: Eizo GmbH
- Inspection Date: 2012-03-28
- 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: 3

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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