FDA Inspection 1051163 — Linemaster Switch Corporation
The FDA completed an inspection of Linemaster Switch Corporation on Apr 12, 2018 in Woodstock, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 12, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Woodstock, CT (United States)