FDA Inspection 1251706 - Veridiam, Inc. - October 10, 2024

FDA Inspection 1251706 for Veridiam, Inc. on October 10, 2024. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1251706 for Veridiam, Inc. on October 10, 2024. Classification: No Action Indicated (NAI).

Violation Codes

21 CFR 820.198(a)

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Record Information

Company

Veridiam, Inc.

Inspection Date

October 10, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff6e384e-a5d4-4147-8611-99070d0d4c92

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