# FDA 483 - InnoMark, Inc. - March 15, 2023

Source: https://www.keypedia.com/records/483/innomark-inc/a13f0d85-5c83-4292-9d22-b0ae5d063b01

> FDA 483 for InnoMark, Inc. on March 15, 2023. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: InnoMark, Inc.
- Inspection Date: 2023-03-15
- Product Type: other
- Office Name: Denver District Office
- Summary: An FDA inspection of InnoMark, Inc. in Saint George, UT, a manufacturer of hot-fill juices and dietary supplements, revealed significant deficiencies. The firm failed to adhere to its HACCP plan, maintain adequate sanitation, and ensure proper quality control for dietary supplements, including identity, purity, strength, and contamination testing. Repeated observations highlight persistent issues with record-keeping and supplier qualification.

## Related Documents

- [WARNING_LETTER - 2023-03-15](https://www.keypedia.com/records/warning_letter/innomark-inc/28535855-9f87-43cd-9b01-f91fdbf5a3d6)

## Related Officers

- [Jennifer A. Robinson](https://www.keypedia.com/people/jennifer-a-robinson/a34d6842-7cc1-4976-8ca7-2b57f1cff756)

Company: https://www.keypedia.com/companies/innomark-inc/76312e60-50df-4408-9c9d-388c15d54fd0

Office: https://www.keypedia.com/offices/denver-district-office/93b79063-390c-4759-af6c-5da7e388face