FDA Inspection 864657 — Contex Inc

Contex Inc — FEI 2017777

The FDA completed an inspection of Contex Inc on January 27, 2014 in Sherman Oaks, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 27, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Sherman Oaks, CA (United States)