# Fiagon GmbH – FDA Inspection, Nov 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/fiagon-gmbh/df70e496-cca9-48f4-98a9-e39d75d9be15
Source feed: FDA_Inspections

> FDA inspection 993512 of Fiagon GmbH, November 10, 2016. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993512
- Company Name: Fiagon GmbH
- Inspection Date: 2016-11-10
- 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 1289434 - 2025-09-11

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/loretta-nemchik/37791f6d-862a-4863-9295-1cca43f9fe3a)

Company: https://www.keypedia.com/companies/fiagon-gmbh/57162fe1-9306-4e19-9001-c67604584a93

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