FDA Inspection 1247165 - Axis Spine Technologies Ltd. - August 21, 2024

FDA Inspection 1247165 for Axis Spine Technologies Ltd. on August 21, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1247165 for Axis Spine Technologies Ltd. on August 21, 2024. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(1)

21 CFR 820.198(a)

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Record Information

Company

Axis Spine Technologies Ltd.

Inspection Date

August 21, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f99e3700-c927-4f83-9ea1-d7e2542cbe80

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