# MED-EL Elektromedizinische Gereate, Gmbh – FDA Inspection, Jun 14, 2012

Source: https://www.keypedia.com/records/fda_inspections/med-el-elektromedizinische-gereate-gmbh/636539ac-fa35-443d-a399-af6c7fb51f90
Source feed: FDA_Inspections

> FDA inspection 791656 of MED-EL Elektromedizinische Gereate, Gmbh, June 14, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791656
- Company Name: MED-EL Elektromedizinische Gereate, Gmbh
- Inspection Date: 2012-06-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

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- FDA Inspection 653048 - 2010-03-22
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Company: https://www.keypedia.com/companies/med-el-elektromedizinische-gereate-gmbh/9de445e0-150e-4574-a05d-db796169a5cf

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