Vi Jon, Inc.January 11, 2017

FDA 483 - Vi Jon, Inc. - January 11, 2017

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Record Details

An FDA inspection of Vi Jon, Inc. in Saint Louis, MO, revealed significant deficiencies in computer system controls and equipment cleaning procedures. The firm's chromatography software allowed unauthorized data deletion and lacked proper procedures for user privileges and audit trail review. Additionally, there was no scientific evidence to support the effectiveness of cleaning procedures for active ingredient removal.

Company: Vi Jon, Inc.
Inspection Date: January 11, 2017
Product Type: Drugs
Office: Division of Human and Animal Food Operations - West II
Person: Tiara N Brown-Crosen

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ID · a7c0b07f-d74f-49fd-945b-266b4260c7c6