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FDA Inspection 946183 — Agilent Technologies, Inc.

Agilent Technologies, Inc. — FEI 2022180

The FDA completed an inspection of Agilent Technologies, Inc. on October 23, 2015 in Carpinteria, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 23, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Carpinteria, CA (United States)

Facility

Other inspections at this facility

  • 1155499 (NAI Wed Sep 29 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1113860 (NAI Fri Dec 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1010582 (VAI Fri Jan 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 947392 (NAI Fri Oct 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 857763 (NAI Thu Dec 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources