FDA Inspection 857763 — Agilent Technologies, Inc.

Agilent Technologies, Inc. — FEI 2022180

The FDA completed an inspection of Agilent Technologies, Inc. on Dec 5, 2013 in Carpinteria, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 5, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Carpinteria, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.