FDA Inspection 675926 — Abbott Laboratories

Abbott Laboratories — FEI 1451914

The FDA completed an inspection of Abbott Laboratories on Jul 27, 2010 in North Chicago, IL. 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 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
North Chicago, IL (United States)

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