FDA Inspection 843058 — Abbott Medical

Abbott Medical — FEI 2017865

The FDA completed an inspection of Abbott Medical on August 1, 2013 in Sylmar, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 1, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sylmar, CA (United States)