# FDA 483 - LNHC Inc. - January 16, 2026

Source: https://www.keypedia.com/records/483/lnhc-inc/c4336315-7c32-4cc6-807d-169da7add4fc

> FDA 483 for LNHC Inc. on January 16, 2026. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: LNHC Inc.
- Inspection Date: 2026-01-16
- Product Type: drugs
- Office Name: Atlanta District Office
- Summary: LNHC Inc. in Durham, NC, was issued a Form 483 following an inspection from January 12-16, 2026. The firm failed to conduct required annual product quality reviews for its active pharmaceutical ingredient (API) since commercial production began in June 2023. This lapse impacts numerous batches that have been released or destroyed without systematic review to verify process consistency.

## Related Officers

- [Yoriann M. Cabrera Bartolomei](https://www.keypedia.com/people/yoriann-m-cabrera-bartolomei/3f827fbc-dcd1-4698-9bae-e0e93b900d08)

Company: https://www.keypedia.com/companies/lnhc-inc/04595a4d-f961-415d-b988-260ca49f71f7

Office: https://www.keypedia.com/offices/atlanta-district-office/7586d99a-288e-49d1-8c3d-d88b7354b7a7