FDA inspection

Vygon US LLC d/b/a Vygon Neuro: FDA inspection ending Jun 26, 2009

FDA inspection 598380 · Voluntary Action Indicated (VAI) · Norristown, PA

Key facts

Inspection ID 598380
Firm Vygon US LLC d/b/a Vygon Neuro
FEI number 2518608
Address 2495 General Armistead Ave
City Norristown
State PA
ZIP 19403
Country United States
Fiscal year 2009
Inspection end date Jun 26, 2009
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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