FDA Inspection 1202546 — Tensentric, LLC

Tensentric, LLC — FEI 3017726824

The FDA completed an inspection of Tensentric, LLC on April 14, 2023 in Louisville, CO. 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
April 14, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Louisville, CO (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures