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