FDA Inspection 1219489 - Stille AB - September 28, 2023

FDA Inspection 1219489 for Stille AB on September 28, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1219489 for Stille AB on September 28, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(a)

21 CFR 820.80(b)

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Record Information

Company

Stille AB

Inspection Date

September 28, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fab244a8-3fe3-48df-b8e8-2b125ba0a107

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