FDA Inspection 916297 - Clariance-SAS - January 29, 2015

FDA Inspection 916297 for Clariance-SAS on January 29, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 916297 for Clariance-SAS on January 29, 2015. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.100(b)

21 CFR 820.198(a)

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Record Information

Company

Clariance-SAS

Inspection Date

January 29, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f753eebc-9d00-4fa5-ae64-9026abeb9ad3

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