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FDA Inspection
•Thoratec LLC•June 12, 2017

Thoratec LLC – FDA Inspection, Jun 12, 2017

Record Details

This FDA Inspection record concerns Thoratec LLC, with an inspection on June 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Thoratec LLC
Inspection Date
June 12, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • James A. Lane (FDA Associated Person)
View Company Profile

ID · 41f1cd12-a813-486b-8661-8ad0ed83d3d0

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1020165
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Thoratec LLC

9
DateClassificationOfficeProject area
May 30, 2025VAISan Francisco District OfficeCompliance: Medical Devices
October 9, 2020NAICenter for Devices and Radiological HealthCompliance: Devices
November 23, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 28, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 15, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
View all 9 other inspections on the company page
Other documents for Thoratec LLC
  • FDA Inspection 1269802 - 2025-05-30
  • FDA Inspection 1132047 - 2020-10-09
  • FDA Inspection 948389 - 2015-11-23
  • FDA Inspection 866589 - 2014-02-28
  • FDA Inspection 839933 - 2013-07-15

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