FDA Inspection 1101815 - Interojo Inc. - August 29, 2019

FDA Inspection 1101815 for Interojo Inc. on August 29, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1101815 for Interojo Inc. on August 29, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.184

21 CFR 820.184(f)

21 CFR 820.75(a)

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Record Information

Company

Interojo Inc.

Inspection Date

August 29, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe72b567-386b-4e3e-847a-491f4a30a1f0

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