FDA Inspection 1030670 — Abbott Laboratories, Inc

Abbott Laboratories, Inc — FEI 1628664

The FDA completed an inspection of Abbott Laboratories, Inc on Jul 24, 2017 in Irving, TX. 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 24, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Irving, TX (United States)

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