FDA Inspection 876439 — Abbott Medical

Abbott Medical — FEI 2017865

The FDA completed an inspection of Abbott Medical on April 11, 2014 in Sylmar, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Sylmar, CA (United States)

Citations

IDCFRDescription
265021 CFR 820.30(f)Design verification - Lack of or inadequate procedures