FDA inspection

Vital Signs Devices, a GE Healthcare Company: FDA inspection ending May 17, 2002

FDA inspection 216356 · No Action Indicated (NAI) · Totowa, NJ

Key facts

Inspection ID 216356
Firm Vital Signs Devices, a GE Healthcare Company
FEI number 2242551
Address 20 Campus Rd
City Totowa
State NJ
ZIP 07512-1210
Fiscal year 2002
Inspection end date May 17, 2002
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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