# FDA 483 - Linemaster Switch Corporation - March 06, 2026

Source: https://www.keypedia.com/records/483/linemaster-switch-corporation/aadc79b9-7ea2-4a98-ad6a-a43a9106211d

> FDA 483 for Linemaster Switch Corporation on March 06, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Linemaster Switch Corporation
- Inspection Date: 2026-03-06
- Product Type: device
- Office Name: New England District Office
- Summary: Linemaster Switch Corporation, a medical device manufacturer in Woodstock, CT, was inspected and cited for significant deficiencies in its quality system. Observations primarily focused on inadequate risk management, insufficient control of nonconforming products, failure to implement corrective actions, and poorly validated environmental controls and software for calibration. These issues pose a risk of unintended laser activation or inadequate laser power delivery from their foot pedal accessory devices.

## Related Documents

- [483 - 2023-02-15](https://www.keypedia.com/records/483/linemaster-switch-corporation/f1617dab-fbd8-4ef1-8fb6-ffff15650c28)
- [WARNING_LETTER - 2026-03-06](https://www.keypedia.com/records/warning_letter/linemaster-switch-corporation/00b08e6b-62ce-40a9-ae39-dfbecb9ed427)

## Related Officers

- [Power Trader/Data Scientist](https://www.keypedia.com/people/jeffrey-j-thibodeau/62b74030-4aef-400b-8ae2-8bf84712d813)

Company: https://www.keypedia.com/companies/linemaster-switch-corporation/651f7d58-aaf7-4ee7-a5d5-320a27d1c4d7

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144