FDA Inspection 860000 — Transonic Systems Inc

Transonic Systems Inc — FEI 1319030

The FDA completed an inspection of Transonic Systems Inc on November 19, 2013 in Ithaca, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 19, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Ithaca, NY (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation