FDA Inspection 1314798 — Televere Systems, LLC

Televere Systems, LLC — FEI 3002906551

The FDA completed an inspection of Televere Systems, LLC on April 22, 2026 in Janesville, WI. 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 22, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Janesville, WI (United States)

Citations

IDCFRDescription
23087ISO 13485:2016 Clause 7.1Product realization risk management processes not documented