FDA Inspection 1046738 — Agilent Technologies, Inc

Agilent Technologies, Inc — FEI 1217454

The FDA completed an inspection of Agilent Technologies, Inc on March 14, 2018 in Winooski, VT. 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
March 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Winooski, VT (United States)