# Medikomp Gmbh – FDA Inspection, Oct 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/medikomp-gmbh/c32bd902-b668-4c05-b045-a85cc32ce894
Source feed: FDA_Inspections

> FDA inspection 992713 of Medikomp Gmbh, October 20, 2016. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992713
- Company Name: Medikomp Gmbh
- Inspection Date: 2016-10-20
- 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: 0

## Related Documents

- FDA Inspection 1273889 - 2025-05-14
- [FDA Inspection 849117 - 2013-08-15](https://www.keypedia.com/records/fda_inspections/medikomp-gmbh/af391f69-52d4-42d1-a2f7-ef0d11fbb392)

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

Company: https://www.keypedia.com/companies/medikomp-gmbh/5f392112-51ba-4c11-9588-95d63626a58f

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