FDA Inspection 960749 - Fareva Morton Grove - February 02, 2016

FDA Inspection 960749 for Fareva Morton Grove on February 02, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 960749 for Fareva Morton Grove on February 02, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Fareva Morton Grove

Inspection Date

February 2, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: b984ad52-0971-427c-b697-052af3ababf2

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