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Companies often get a 483 for a deviation investigation process deficiency. Here's why training is needed:
- Teams can't solve problems, get results, or comply with FDA expectations for thorough deviation investigations.
To learn more:
- call Allan Dewes (415-948-5220), or
- visit http://www.skillsplusinc.com/root_cause.htm
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SkillsPlus Intl Inc. - The Best GMP & QSR Compliance Training Around
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