FDA Inspection 716720 — Abbott Laboratories

Abbott Laboratories — FEI 2919069

The FDA completed an inspection of Abbott Laboratories on Apr 1, 2011 in Santa Clara, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 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

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