# FDA 483 - LICO Industries, LLC - February 19, 2026

Source: https://www.keypedia.com/records/483/lico-industries-llc/121ffc53-d5b7-43b5-81cf-3e809248e421

> FDA 483 for LICO Industries, LLC on February 19, 2026. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: LICO Industries, LLC
- Inspection Date: 2026-02-19
- Product Type: drugs
- Office Name: FDA District Office — Denver, Colorado
- Summary: LICO Industries, LLC, a repackager and relabeler of OTC drug products in Mohave Valley, AZ, was cited for significant deficiencies during an FDA inspection. The inspection revealed a lack of an adequate quality control unit, failure to test incoming components for identity, and inadequate production and process controls, including issues with process and cleaning validation. These repeat observations indicate serious and systemic quality control failures.

## Related Documents

- [483 - 2021-07-08](https://www.keypedia.com/records/483/lico-industries-llc/fa1dd772-3b60-4a9c-8269-51b3c9fe7188)

## Related Officers

- [Hung H. Do](https://www.keypedia.com/people/hung-h-do/580f78ba-ed7a-4c10-8f4c-a99d0af7206e)

Company: https://www.keypedia.com/companies/lico-industries-llc/414190d6-ef0c-476d-b553-437370b636eb

Office: https://www.keypedia.com/offices/fda-district-office-denver-colorado/1670d160-cbfd-48fd-b9c1-fbba4631fcb0