FDA Inspection 1091806 - Clariance Inc - June 04, 2019

FDA Inspection 1091806 for Clariance Inc on June 04, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1091806 for Clariance Inc on June 04, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17(a)(2)

21 CFR 803.50(a)(2)

21 CFR 806.20(b)(4)

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.40

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Record Information

Company

Clariance Inc

Inspection Date

June 4, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fce3ec09-e267-4696-b661-2a9e0b902e65

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