FDA Inspection 1010435 — Domex Technology Corporation
The FDA completed an inspection of Domex Technology Corporation on April 12, 2017 in Hsinchu. 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
- April 12, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hsinchu (Taiwan)