FDA Inspection
Fiagon GmbHFiagon GmbH – FDA Inspection, Nov 10, 2016
Record Details
This FDA Inspection record concerns Fiagon GmbH, with an inspection on November 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · df70e496-cca9-48f4-98a9-e39d75d9be15
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 993512
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Fiagon GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2025 | Not classified | Office of Inspections and Investigations |
Other documents for Fiagon GmbH
- FDA Inspection 1289434 - 2025-09-11
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