FDA inspection

Mediplast Israel Ltd.: FDA inspection ending Aug 31, 2017

FDA inspection 1035247 · Voluntary Action Indicated (VAI) · Yavne

Key facts

Inspection ID 1035247
Firm Mediplast Israel Ltd.
FEI number 3002807555
Address Industrial Area, 7, Ha-Yarkon
City Yavne
Country Israel
Fiscal year 2017
Inspection end date Aug 31, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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