# FDA 483 - Vi Jon, Inc. - September 14, 2010

Source: https://www.globalkeysolutions.net/records/483/vi-jon-inc/81572f08-155d-44a2-a990-6dd834b6411b

> FDA 483 for Vi Jon, Inc. on September 14, 2010. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Vi Jon, Inc.
- Inspection Date: 2010-09-14
- Product Type: drugs
- Office Name: Kansas City District Office
- Summary: An FDA inspection of Vi-Jon, Inc. in St. Louis, MO, an OTC drug and cosmetic manufacturer, identified a significant failure in their quality control processes. The firm did not conduct out-of-specification (OOS) investigations for Total Organic Carbon (TOC) in water samples that exceeded established limits. Furthermore, the company lacked a formal OOS procedure for investigating TOC deviations, indicating a critical gap in their manufacturing controls.

## Related Documents

- [483 - 2017-01-11](https://www.globalkeysolutions.net/records/483/vi-jon-inc/a7c0b07f-d74f-49fd-945b-266b4260c7c6)

## Related Officers

- [Adree Anderson](https://www.globalkeysolutions.net/people/adree-anderson/c6c78249-62ae-4c4a-bb91-476093e74e53)

Company: https://www.globalkeysolutions.net/companies/vi-jon-inc/e0966124-67b8-4646-93a7-760565a90cd2

Office: https://www.globalkeysolutions.net/offices/kansas-city-district-office/cd397ab1-df4e-46f1-ab1c-0f6db9abcf79