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FDA Inspection
•Varian Medical Systems, Inc.•May 20, 2015

Varian Medical Systems, Inc. – FDA Inspection, May 20, 2015

Record Details

This FDA Inspection record concerns Varian Medical Systems, Inc., with an inspection on May 20, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Varian Medical Systems, Inc.
Inspection Date
May 20, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c5597790-cfb8-4a39-91d9-9e1441367d2b

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
928587
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 803.50(a)(1)Report of Death or Serious Injury
  2. 21 CFR 820.100(b)Documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Varian Medical Systems, Inc.

3
DateClassificationOfficeProject area
October 19, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
November 18, 2009OAICenter for Devices and Radiological HealthCompliance: Devices
February 10, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Varian Medical Systems, Inc.
  • FDA Inspection 752321 - 2011-10-19
  • FDA Inspection 631790 - 2009-11-18
  • FDA Inspection 567174 - 2009-02-10

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