FDA Inspection 931750 - IQVIA - June 19, 2015

FDA Inspection 931750 for IQVIA on June 19, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 931750 for IQVIA on June 19, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

IQVIA

Inspection Date

June 19, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 1a4fdfb5-ae64-4887-afcc-08022e9e52bd

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