FDA Inspection 1216778 - ECTOSENSE NV - August 31, 2023

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Record Details

This FDA Inspection record concerns ECTOSENSE NV, with an inspection on August 31, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: ECTOSENSE NV
Inspection Date: August 31, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · bdaf415a-e33b-4359-b082-fae9285b961d

Violation Codes3

21 CFR 820.5021 CFR 820.80(d)21 CFR 820.90(a)

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