FDA Inspection 1319444 — Agilent Technologies Inc

Agilent Technologies Inc — FEI 3007057070

The FDA completed an inspection of Agilent Technologies Inc on May 6, 2026 in Boulder, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 6, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Boulder, CO (United States)

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