FDA inspection

Mediplast Israel Ltd.: FDA inspection ending Jul 17, 2002

FDA inspection 234502 · Voluntary Action Indicated (VAI) · Yavne

Key facts

Inspection ID 234502
Firm Mediplast Israel Ltd.
FEI number 3002807555
Address Industrial Area, 7, Ha-Yarkon
City Yavne
Fiscal year 2002
Inspection end date Jul 17, 2002
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None 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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