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FDA Inspection 947392 — 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 NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 23, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Carpinteria, CA (United States)

Additional Details

Sponsor, Contract Research Organization

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))
  • 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