FDA inspection

Oridion Medical 1987 Ltd.: FDA inspection ending May 2, 2012

FDA inspection 780722 · No Action Indicated (NAI) · Jerusalem

Key facts

Inspection ID 780722
Firm Oridion Medical 1987 Ltd.
FEI number 3001227743
Address Har Hotzvim Industrial Park Box 45025, Har Hotzvim Industrial Park
City Jerusalem
Country Israel
Fiscal year 2012
Inspection end date May 2, 2012
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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