FDA Inspection 1260145 - Keranetics Inc. - February 06, 2025

FDA Inspection 1260145 for Keranetics Inc. on February 06, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1260145 for Keranetics Inc. on February 06, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 820.22

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Record Information

Company

Keranetics Inc.

Inspection Date

February 6, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe859a91-8a3e-478f-9f47-8e984e72eabd

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