# FDA Inspection 993512 - Fiagon GmbH - November 10, 2016

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

> FDA Inspection 993512 for Fiagon GmbH on November 10, 2016. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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