FDA Inspection 914699 — Agilent Technologies Denmark ApS

Agilent Technologies Denmark ApS — FEI 3002806778

The FDA completed an inspection of Agilent Technologies Denmark ApS on January 15, 2015 in Glostrup. 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
January 15, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Glostrup (Denmark)