FDA Inspection 1239139 - Perfuze LTD - May 22, 2024

FDA Inspection 1239139 for Perfuze LTD on May 22, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1239139 for Perfuze LTD on May 22, 2024. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.250(a)

21 CFR 820.70(e)

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Record Information

Company

Perfuze LTD

Inspection Date

May 22, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fde0c7a3-8ebb-4fe0-ad26-47ffcc84eeb5

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