FDA Inspection 989089 — Bioteque Corporation I-Lan Factory II
The FDA completed an inspection of Bioteque Corporation I-Lan Factory II on July 15, 2016 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
- July 15, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Su-Ao Cheng (Taiwan)