FDA inspection

Vygon GmbH & Co. KG: FDA inspection ending Jan 29, 2015

FDA inspection 914889 · Voluntary Action Indicated (VAI) · Aachen

Key facts

Inspection ID 914889
Firm Vygon GmbH & Co. KG
FEI number 3002808464
Address Prager Ring 100
City Aachen
Country Germany
Fiscal year 2015
Inspection end date Jan 29, 2015
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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