FDA Inspection 1260617 - Ortec - January 09, 2025

FDA Inspection 1260617 for Ortec on January 09, 2025. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1260617 for Ortec on January 09, 2025. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.30(a)

21 CFR 820.50

21 CFR 820.75(a)

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Record Information

Company

Ortec

Inspection Date

January 9, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbd92500-709f-409c-a1e1-a0effe612d26

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