FDA Inspection 1067530 - Avista Pharma Solutions, Inc. dba Cambrex - September 05, 2018

FDA Inspection 1067530 for Avista Pharma Solutions, Inc. dba Cambrex on September 05, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1067530 for Avista Pharma Solutions, Inc. dba Cambrex on September 05, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Avista Pharma Solutions, Inc. dba Cambrex

Inspection Date

September 5, 2018

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: d175dd6d-7561-482d-b246-920920a41ec5

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