FDA Inspection 1000203 - MasterPharm LLC - January 30, 2017

FDA Inspection 1000203 for MasterPharm LLC on January 30, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1000203 for MasterPharm LLC on January 30, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

MasterPharm LLC

Inspection Date

January 30, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: ed46c4aa-20ad-4b33-901e-c3e687aa3527

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