FDA Inspection 663582 - ActiTech, LP - May 24, 2010

FDA Inspection 663582 for ActiTech, LP on May 24, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 663582 for ActiTech, LP on May 24, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.100(a)

21 CFR 211.160(a)

21 CFR 211.180(e)

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Record Information

Company

ActiTech, LP

Inspection Date

May 24, 2010

Product Type

Cosmetics

Office

Center for Food Safety and Applied Nutrition

ID: ff8e8b53-d1bb-4af4-a245-415548c80605

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