FDA Inspection 1250056 - Enestia Belgium NV - September 19, 2024
FDA Inspection 1250056 for Enestia Belgium NV on September 19, 2024. Classification: VAI.
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FDA Inspection 1250056 for Enestia Belgium NV on September 19, 2024. Classification: VAI.
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Company
Enestia Belgium NVInspection Date
September 19, 2024
Product Type
Medical Devices & Rad Health
ID: 917c3608-36f0-4545-8b1f-144fc2530d7d
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