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FDA Inspection
•Transonic Systems Inc•March 21, 2013

Transonic Systems Inc – FDA Inspection, Mar 21, 2013

Record Details

This FDA Inspection record concerns Transonic Systems Inc, with an inspection on March 21, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Transonic Systems Inc
Inspection Date
March 21, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · f87181a8-e810-41f3-a846-d0c3b42dc9d9

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
823936
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Transonic Systems Inc

4
DateClassificationOfficeProject area
February 1, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 16, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
November 19, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
January 26, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Transonic Systems Inc
  • FDA Inspection 1040245 - 2018-02-01
  • FDA Inspection 1015982 - 2017-06-16
  • FDA Inspection 860000 - 2013-11-19
  • FDA Inspection 643524 - 2010-01-26

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