FDA Inspection 1010306 — Abbott Point Of Care Canada Limited

Abbott Point Of Care Canada Limited — FEI 3005643513

The FDA completed an inspection of Abbott Point Of Care Canada Limited on Oct 20, 2016 in Nepean. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 20, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Nepean (Canada)

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