FDA Inspection 554108 — Tricor Systems

Tricor Systems — FEI 3001451660

The FDA completed an inspection of Tricor Systems on October 9, 2008 in Elgin, IL. 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
October 9, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Elgin, IL (United States)

Citations

IDCFRDescription
316721 CFR 820.198(a)Complete files maintained