# FDA 483 - Trividia Manufacturing Solutions, Inc. - March 06, 2025

Source: https://www.globalkeysolutions.net/records/483/trividia-manufacturing-solutions-inc/69e8024e-b793-4b07-8b71-d1aef163aea7

> FDA 483 for Trividia Manufacturing Solutions, Inc. on March 06, 2025. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Trividia Manufacturing Solutions, Inc.
- Inspection Date: 2025-03-06
- Product Type: drugs
- Office Name: New England District Office
- Summary: Trividia Manufacturing Solutions, Inc. in Lancaster, NH, was inspected and received a Form 483 with four observations. The inspection revealed significant issues including inadequate investigation and timely closure of out-of-specification results, deficient verification of testing methods, and a lack of proper employee training for critical manufacturing tasks. Additionally, the firm's complaint handling procedures were found to be severely lacking, potentially impacting product quality and patient safety.

## Related Officers

- [Deputy Director](https://www.globalkeysolutions.net/people/lori-m-newman/a0e448e4-11ba-4095-b879-feabb8750b3f)

Company: https://www.globalkeysolutions.net/companies/trividia-manufacturing-solutions-inc/b9682c2e-95cd-45f8-94be-9f0999ee0c83

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