FDA Inspection 1199731 — Linemaster Switch Corporation

Linemaster Switch Corporation — FEI 3001592626

The FDA completed an inspection of Linemaster Switch Corporation on February 15, 2023 in Woodstock, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 15, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Woodstock, CT (United States)