FDA Inspection 993512 — Fiagon GmbH
The FDA completed an inspection of Fiagon GmbH on November 10, 2016 in Hennigsdorf. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- November 10, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hennigsdorf (Germany)