FDA Inspection 1250056 - Enestia Belgium NV - September 19, 2024

FDA Inspection 1250056 for Enestia Belgium NV on September 19, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1250056 for Enestia Belgium NV on September 19, 2024. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.70(i)

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Record Information

Company

Enestia Belgium NV

Inspection Date

September 19, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 3793d9b3-5e59-4b44-80fe-222ce9d0caa1

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