FDA Inspection 1100255 — Agilent Technologies Inc

Agilent Technologies Inc — FEI 3014531850

The FDA completed an inspection of Agilent Technologies Inc on August 7, 2019 in Frederick, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 7, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frederick, CO (United States)