FDA Inspection 977267 - Intelerad USA - June 29, 2016

FDA Inspection 977267 for Intelerad USA on June 29, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 977267 for Intelerad USA on June 29, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Intelerad USA

Inspection Date

June 29, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f80a9f7f-c4c9-45f6-92c8-b338ce5d1e98

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