FDA inspection

Philips Commercial France SAS: FDA inspection ending Jul 12, 2018

FDA inspection 1059711 · Voluntary Action Indicated (VAI) · Paris

Key facts

Inspection ID 1059711
Firm Philips Commercial France SAS
FEI number 3003630387
Address 76 Avenue De France
City Paris
Country France
Fiscal year 2018
Inspection end date Jul 12, 2018
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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