FDA Inspection 1289902 - Retmap Inc - October 30, 2025

FDA Inspection 1289902 for Retmap Inc on October 30, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1289902 for Retmap Inc on October 30, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.20(c)

21 CFR 820.22

21 CFR 820.50(a)(3)

21 CFR 820.72(a)

21 CFR 820.90(a)

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Record Information

Company

Retmap Inc

Inspection Date

October 30, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f857a39f-98d2-409b-858f-f32da9b3c78f

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