FDA inspection

Biosense Webster, Inc.: FDA inspection ending Sep 27, 2016

FDA inspection 991212 · No Action Indicated (NAI) · Irwindale, CA

Key facts

Inspection ID 991212
Firm Biosense Webster, Inc.
FEI number 3003113629
Address 15715 Arrow Hwy
City Irwindale
State CA
ZIP 91706
Country United States
Fiscal year 2016
Inspection end date Sep 27, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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

Browse all FDA inspections