FDA Inspection 1275926 — Agilent Technologies Inc

Agilent Technologies Inc — FEI 3014531850

The FDA completed an inspection of Agilent Technologies Inc on Jun 18, 2025 in Frederick, 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
Jun 18, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frederick, CO (United States)

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