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FDA Inspection 823936 — Transonic Systems Inc

Transonic Systems Inc — FEI 1319030

The FDA completed an inspection of Transonic Systems Inc on March 21, 2013 in Ithaca, NY. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ithaca, NY (United States)

Facility

Other inspections at this facility

  • 1040245 (VAI Thu Feb 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1015982 (VAI Fri Jun 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 860000 (VAI Tue Nov 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 643524 (VAI Tue Jan 26 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources