FDA Inspection 1276832 - ARCHFORM INC - July 28, 2025

FDA Inspection 1276832 for ARCHFORM INC on July 28, 2025. Classification: VAI.

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Record Summary

FDA Inspection 1276832 for ARCHFORM INC on July 28, 2025. Classification: VAI.

Violation Codes

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.90(a)

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Record Information

Company

ARCHFORM INC

Inspection Date

July 28, 2025

Product Type

Medical Devices & Rad Health

Office

San Francisco District Office

ID: fede2953-bb29-4023-bf53-fc85eff12f09

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