FDA Inspection 1017182 — Abbott Laboratories

Abbott Laboratories — FEI 2919069

The FDA completed an inspection of Abbott Laboratories on May 17, 2017 in Santa Clara, CA. 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
May 17, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)

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