FDA Inspection 943637 — Baxter Corporation

Baxter Corporation — FEI 3002891260

The FDA completed an inspection of Baxter Corporation on Jul 30, 2015 in Alliston. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Alliston (Canada)

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