FDA Inspection 1262847 - Neosoma, Inc. - February 21, 2025

FDA Inspection 1262847 for Neosoma, Inc. on February 21, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1262847 for Neosoma, Inc. on February 21, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.181

21 CFR 820.184

21 CFR 820.90(b)(1)

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Record Information

Company

Neosoma, Inc.

Inspection Date

February 21, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdf95124-3f4e-4906-bae2-9669f5f5a31f

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