FDA Inspection 1019474 - Hologic, Inc. - July 28, 2017

FDA Inspection 1019474 for Hologic, Inc. on July 28, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1019474 for Hologic, Inc. on July 28, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 1002.20(a)

21 CFR 1002.30(a)(1)

21 CFR 1002.30(a)(2)

21 CFR 1003.10(a)

21 CFR 1020.30(g)

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Record Information

Company

Hologic, Inc.

Inspection Date

July 28, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f69118a5-b6c1-4363-8bbc-a0090ccee864

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