FDA Inspection 798314 — Agilent Technologies, Inc

Agilent Technologies, Inc — FEI 1217454

The FDA completed an inspection of Agilent Technologies, Inc on August 15, 2012 in Winooski, VT. 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
August 15, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Winooski, VT (United States)

Citations

IDCFRDescription
243021 CFR 820.30(b)Design plans - Lack of or inadequate