FDA inspection

Intermedic Arfran S.A.: FDA inspection ending Feb 5, 2016

FDA inspection 958881 · Voluntary Action Indicated (VAI) · Cerdanyola Del Valles

Key facts

Inspection ID 958881
Firm Intermedic Arfran S.A.
FEI number 3008206114
Address Calle Dels Boters 8-10
City Cerdanyola Del Valles
Country Spain
Fiscal year 2016
Inspection end date Feb 5, 2016
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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