FDA Inspection 1264423 — Bioteque Corporation I-Lan Factory II

Bioteque Corporation I-Lan Factory II — FEI 3004207966

The FDA completed an inspection of Bioteque Corporation I-Lan Factory II on June 12, 2025 in Su-Ao Cheng. 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
June 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Su-Ao Cheng (Taiwan)