FDA inspection

Orthofix Srl: FDA inspection ending Sep 27, 2012

FDA inspection 802729 · Voluntary Action Indicated (VAI) · Bussolengo

Key facts

Inspection ID 802729
Firm Orthofix Srl
FEI number 3002807827
Address Via Delle Nazioni 9
City Bussolengo
Country Italy
Fiscal year 2012
Inspection end date Sep 27, 2012
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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