FDA Inspection 1016272 - Alung Technologies Inc - March 16, 2017

FDA Inspection 1016272 for Alung Technologies Inc on March 16, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1016272 for Alung Technologies Inc on March 16, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(1)

21 CFR 803.50(a)(2)

21 CFR 820.100(a)

21 CFR 820.100(b)

21 CFR 820.198(a)

21 CFR 820.198(e)

21 CFR 820.200(c)

21 CFR 820.75(b)

21 CFR 820.75(b)(2)

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Record Information

Company

Alung Technologies Inc

Inspection Date

March 16, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6ceb5ae-fb2a-40d5-acd7-7e66457cb754

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