FDA inspection

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: FDA inspection ending Nov 20, 2008

FDA inspection 551807 · Voluntary Action Indicated (VAI) · Best

Key facts

Inspection ID 551807
Firm PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FEI number 3002807880
Address Veenpluis 4-6
City Best
Country Netherlands
Fiscal year 2009
Inspection end date Nov 20, 2008
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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