FDA Inspection 1058626 - ScandiDos AB - July 12, 2018

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Record Details

This FDA Inspection record concerns ScandiDos AB, with an inspection on July 12, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: ScandiDos AB
Inspection Date: July 12, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 98c1110b-a4e4-4f05-8011-e49b1326151d

Violation Codes4

21 CFR 820.18421 CFR 820.30(h)21 CFR 820.80(b)21 CFR 820.90(a)

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