FDA Inspection 1208833 - NEOSS AB - June 27, 2023

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Record Details

This FDA Inspection record concerns NEOSS AB, with an inspection on June 27, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: NEOSS AB
Inspection Date: June 27, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dd592a8f-88a0-4ed3-9ff4-5f3014e0520c

Violation Codes2

21 CFR 820.198(a)21 CFR 820.22

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