FDA inspection

Agilent Technologies: FDA inspection ending Dec 29, 2003

FDA inspection 310687 · No Action Indicated (NAI) · Loveland, CO

Key facts

Inspection ID 310687
Firm Agilent Technologies
FEI number 1718499
Address 815 14th St Sw
City Loveland
State CO
ZIP 80537-6330
Fiscal year 2004
Inspection end date Dec 29, 2003
Classification No Action Indicated (NAI)
Project area Rad Cntrl & Hlth Safety Act (RCHSA) Auth
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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