FDA Inspection 1253044 - Medtronic CryoCath LP - October 31, 2024

FDA Inspection 1253044 for Medtronic CryoCath LP on October 31, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1253044 for Medtronic CryoCath LP on October 31, 2024. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.86

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Record Information

Company

Medtronic CryoCath LP

Inspection Date

October 31, 2024

Product Type

Devices

ID: fe726b2b-3a74-4fb9-8b39-eb444aea9976

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