FDA Inspection 1249530 - BIOTEC ITALIA - August 08, 2024

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Record Details

This FDA Inspection record concerns BIOTEC ITALIA, with an inspection on August 8, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: BIOTEC ITALIA
Inspection Date: August 8, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 04cc9729-4b46-4e72-9702-98b9f58e26c0

Violation Codes2

21 CFR 820.198(a)21 CFR 820.30(g)

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