FDA Inspection 988732 - Avista Pharma Solutions, Inc. dba Cambrex - June 15, 2016

FDA Inspection 988732 for Avista Pharma Solutions, Inc. dba Cambrex on June 15, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 988732 for Avista Pharma Solutions, Inc. dba Cambrex on June 15, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Avista Pharma Solutions, Inc. dba Cambrex

Inspection Date

June 15, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: c88cfac6-d9aa-4a5a-adc0-be20464a8181

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