FDA Inspection 993512 — Fiagon GmbH
The FDA completed an inspection of Fiagon GmbH on Nov 10, 2016 in Hennigsdorf. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 10, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hennigsdorf (Germany)