FDA Inspection 711086 — Tricor Systems

Tricor Systems — FEI 3001451660

The FDA completed an inspection of Tricor Systems on February 24, 2011 in Elgin, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 24, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Elgin, IL (United States)