FDA Inspection 716720 — Abbott Laboratories

Abbott Laboratories — FEI 2919069

The FDA completed an inspection of Abbott Laboratories on April 1, 2011 in Santa Clara, 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 1, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)

Citations

IDCFRDescription
312821 CFR 820.90(a)Nonconforming product control