FDA Inspection 1264311 — Visgeneer, Inc.

Visgeneer, Inc. — FEI 3005644014

The FDA completed an inspection of Visgeneer, Inc. on February 27, 2025 in Hsinchu City. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 27, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Hsinchu City (Taiwan)