# Elexxion AG – FDA Inspection, Feb 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/elexxion-ag/e58eb232-3d90-4f01-98f7-504a414d264b
Source feed: FDA_Inspections

> FDA inspection 772059 of Elexxion AG, February 16, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 772059
- Company Name: Elexxion AG
- Inspection Date: 2012-02-16
- 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: 2

Company: https://www.keypedia.com/companies/elexxion-ag/237aaeaa-4e2d-47ca-83ff-230964eb341a

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