FDA inspection

Biosense Webster (israel), Ltd.: FDA inspection ending Oct 26, 2017

FDA inspection 1045659 · No Action Indicated (NAI) · Yoqne'Am Illit

Key facts

Inspection ID 1045659
Firm Biosense Webster (israel), Ltd.
FEI number 3008203003
Address 4, Hatnufah Street
City Yoqne'Am Illit
Fiscal year 2018
Inspection end date Oct 26, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None 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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