# MED-EL Elektromedizinische Gereate, Gmbh – FDA Inspection, May 7, 2015

Source: https://www.keypedia.com/records/fda_inspections/med-el-elektromedizinische-gereate-gmbh/f3caf7b8-24c3-4759-8c09-309ad1251ec8
Source feed: FDA_Inspections

> FDA inspection 925871 of MED-EL Elektromedizinische Gereate, Gmbh, May 07, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 925871
- Company Name: MED-EL Elektromedizinische Gereate, Gmbh
- Inspection Date: 2015-05-07
- 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: 1

## Related Documents

- [FDA Inspection 791656 - 2012-06-14](https://www.keypedia.com/records/fda_inspections/med-el-elektromedizinische-gereate-gmbh/636539ac-fa35-443d-a399-af6c7fb51f90)
- FDA Inspection 653048 - 2010-03-22
- FDA Inspection 634572 - 2009-11-26

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