FDA Inspection 1264311 — Visgeneer, Inc.

Visgeneer, Inc. — FEI 3005644014

The FDA completed an inspection of Visgeneer, Inc. on Feb 27, 2025 in Hsinchu City. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.