# FDA 483 - West-Conn Tool & Die Inc. - November 10, 2022

Source: https://www.keypedia.com/records/483/west-conn-tool-die-inc/212c8730-f356-452d-94c6-f3742e94d6cc

> FDA 483 for West-Conn Tool & Die Inc. on November 10, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: West-Conn Tool & Die Inc.
- Inspection Date: 2022-11-10
- Product Type: device
- Office Name: Division of Northeast Imports 
- Summary: West-Conn Tool & Die Inc., a contract manufacturer in Shelton, CT, received a Form FDA 483 with one observation. The inspection revealed that the firm failed to adequately establish schedules for equipment maintenance. Specifically, preventative maintenance for a laser engraver used for medical device components had not been documented since November 2020.

## Related Officers

- [Katarzyna Plona](https://www.keypedia.com/people/katarzyna-plona/ea20d6c6-5d2d-41a0-a755-0647fb9f3250)

Company: https://www.keypedia.com/companies/west-conn-tool-die-inc/b1acd024-4cc0-4c28-a5f5-ef7ea19e6e89

Office: https://www.keypedia.com/offices/division-of-northeast-imports/b20599cf-9797-41fd-947f-6589ef596a94