FDA inspection

Orthofix U.S. LLC: FDA inspection ending Mar 17, 2023

FDA inspection 1200226 · Voluntary Action Indicated (VAI) · Lewisville, TX

Key facts

Inspection ID 1200226
Firm Orthofix U.S. LLC
FEI number 2183449
Address 3451 Plano Pkwy
City Lewisville
State TX
ZIP 75056
Country United States
Fiscal year 2023
Inspection end date Mar 17, 2023
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
  • 10–99 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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