FDA inspection

Vygon Portugal - Produtos Medicos e Farmaceuticos, Lda: FDA inspection ending Apr 11, 2024

FDA inspection 1237846 · Voluntary Action Indicated (VAI) · Baltar

Key facts

Inspection ID 1237846
Firm Vygon Portugal - Produtos Medicos e Farmaceuticos, Lda
FEI number 3014663754
Address Parque Empresarial De Parada/Baltar
City Baltar
Country Portugal
Fiscal year 2024
Inspection end date Apr 11, 2024
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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