# FDA Inspection 1058626 - ScandiDos AB - July 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/scandidos-ab/98c1110b-a4e4-4f05-8011-e49b1326151d
Source feed: FDA_Inspections

> FDA Inspection 1058626 for ScandiDos AB on July 12, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058626
- Company Name: ScandiDos AB
- Inspection Date: 2018-07-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/scandidos-ab/8a121d76-151b-4e72-b3da-c6415ebaf094

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7