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•ARCHEON•September 19, 2025

FDA Inspection 1286532 - ARCHEON - September 19, 2025

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Record Details

This FDA Inspection record concerns ARCHEON, with an inspection on September 19, 2025, covering devices.

Company: ARCHEON
Inspection Date: September 19, 2025
Product Type: Devices

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ID · c36199e8-4c7d-4181-83af-c7e5bd4afb51

Violation Codes2

21 CFR 806.20(b)(4)21 CFR 820.198(a)

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FDA Inspection 1286532 - ARCHEON - September 19, 2025 | Global Key Solutions