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FDA Inspection
•Torax Medical, Inc.•November 8, 2016

Torax Medical, Inc. – FDA Inspection, Nov 8, 2016

Record Details

This FDA Inspection record concerns Torax Medical, Inc., with an inspection on November 8, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Torax Medical, Inc.
Inspection Date
November 8, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kyle J. Mccracken (FDA Associated Person)
View Company Profile

ID · ccf65c82-7b9e-4b44-940a-c2df5b2e4b33

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
991763
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Torax Medical, Inc.

6
DateClassificationOfficeProject area
November 19, 2025NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 16, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 20, 2020NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 28, 2013NAICenter for Devices and Radiological HealthBioresearch Monitoring
March 14, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
View all 6 other inspections on the company page
Other documents for Torax Medical, Inc.
  • FDA Inspection 1291992 - 2025-11-19
  • FDA Inspection 1223685 - 2023-11-16
  • FDA Inspection 1120010 - 2020-02-20
  • FDA Inspection 825848 - 2013-03-28
  • FDA Inspection 714721 - 2011-03-14

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