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 Jun 12, 2025 in Su-Ao Cheng. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Su-Ao Cheng (Taiwan)

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