FDA Inspection 845155 — Abbott Medical

Abbott Medical — FEI 3007113487

The FDA completed an inspection of Abbott Medical on Aug 22, 2013 in Saint Paul, MN. 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
Aug 22, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

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