FDA Inspection 1199731 — Linemaster Switch Corporation

Linemaster Switch Corporation — FEI 3001592626

The FDA completed an inspection of Linemaster Switch Corporation on Feb 15, 2023 in Woodstock, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.