FDA Inspection 1240179 — TriMed Inc.

TriMed Inc. — FEI 3001236812

The FDA completed an inspection of TriMed Inc. on June 3, 2024 in Valencia, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 3, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Valencia, CA (United States)

Citations

IDCFRDescription
367621 CFR 820.30(f)Design verification - documentation
369621 CFR 820.100(b)Documentation