# Eizo GmbH – FDA Inspection, Sep 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/eizo-gmbh/b2657542-6120-4376-ada4-76673d50c58d
Source feed: FDA_Inspections

> FDA inspection 1066467 of Eizo GmbH, September 20, 2018. Classification: No Action Indicated (NAI). 6 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066467
- Company Name: Eizo GmbH
- Inspection Date: 2018-09-20
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

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- [FDA Inspection 779687 - 2012-03-28](https://www.keypedia.com/records/fda_inspections/eizo-gmbh/b3b048ed-28f0-401a-8515-040eb1dde590)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

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