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FDA Inspection 1113860 — Agilent Technologies, Inc.

Agilent Technologies, Inc. — FEI 2022180

The FDA completed an inspection of Agilent Technologies, Inc. on December 6, 2019 in Carpinteria, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 6, 2019
Fiscal Year
2020
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))
  • 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))
  • 946183 (VAI 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