FDA Inspection 703154 — Abaxis Inc

Abaxis Inc — FEI 2939693

The FDA completed an inspection of Abaxis Inc on December 22, 2010 in Union City, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 22, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Union City, CA (United States)

Citations

IDCFRDescription
314921 CFR 820.180Availability