# FDA 483 - Zarbee's Inc - December 11, 2017

Source: https://www.keypedia.com/records/483/zarbees-inc/35194fb7-ee7d-4e89-8ff0-6de294e42c8a

> FDA 483 for Zarbee's Inc on December 11, 2017. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Zarbee's Inc
- Inspection Date: 2017-12-11
- Product Type: other
- Office Name: Denver District Office
- Summary: An FDA inspection of Zarbee's Inc., a dietary supplement own label distributor in Draper, UT, revealed a significant quality control deficiency. The firm failed to ensure finished batches of Infant Gripe Water conformed to product specifications, relying on an unverified "Quantified by Input" method. This practice lacked proper documentation and scientific justification, raising concerns about product quality and regulatory compliance.

## Related Documents

- [483 - 2015-06-17](https://www.keypedia.com/records/483/zarbees-inc/35b26804-4dc7-4a99-96ee-298ff6883634)
- [483 - 2015-07-09](https://www.keypedia.com/records/483/zarbees-inc/2f5b375f-1d79-453c-812d-d5e26114a8b4)

## Related Officers

- [Matthew A. Johnson](https://www.keypedia.com/people/matthew-a-johnson/e94e2d6a-1705-4ba4-b777-d514970e5371)

Company: https://www.keypedia.com/companies/zarbees-inc/0ca5d801-6f18-4c66-ad4d-08b113139c7e

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