FDA inspection

Ortheon Medical: FDA inspection ending Mar 15, 2011

FDA inspection 713975 · Voluntary Action Indicated (VAI) · Columbus, OH

Key facts

Inspection ID 713975
Firm Ortheon Medical
FEI number 3003745909
Address 777 W Swan St
City Columbus
State OH
ZIP 43212
Country United States
Fiscal year 2011
Inspection end date Mar 15, 2011
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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