FDA Inspection 1105962 - InterValve Medical, Inc - September 12, 2019

FDA Inspection 1105962 for InterValve Medical, Inc on September 12, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1105962 for InterValve Medical, Inc on September 12, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

InterValve Medical, Inc

Inspection Date

September 12, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb772af6-7dfc-4453-9890-0b0dec26372a

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