FDA Inspection 703154 — Abaxis Inc

Abaxis Inc — FEI 2939693

The FDA completed an inspection of Abaxis Inc on Dec 22, 2010 in Union City, CA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

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

Citations

IDCFRDescription
314921 CFR 820.180Availability

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