FDA Inspection 1050135 — Trillium Technology, Inc.

Trillium Technology, Inc. — FEI 3007457520

The FDA completed an inspection of Trillium Technology, Inc. on Apr 30, 2018 in Peoria, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 30, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Peoria, IL (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate