FDA Warning Letter — Abaxis Inc

Case 558421 — FEI 2939693

The FDA took a Warning Letter action against Abaxis Inc on Apr 12, 2019 (Union City, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Abaxis Inc
Date
Apr 12, 2019
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Union City, CA (United States)

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