# FDA Inspection 1047590 - Elos Medtech Skara AB - March 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-skara-ab/78ae3148-bbc4-45be-a2b5-57db3949ff53
Source feed: FDA_Inspections

> FDA Inspection 1047590 for Elos Medtech Skara AB on March 23, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047590
- Company Name: Elos Medtech Skara AB
- Inspection Date: 2018-03-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1220692 - 2023-08-31](https://www.keypedia.com/records/fda_inspections/elos-medtech-skara-ab/3fb5c228-7668-4fe9-9d15-5ecbe9814d5a)
- [FDA Inspection 1047590 - 2018-03-23](https://www.keypedia.com/records/fda_inspections/elos-medtech-skara-ab/e88cc382-923f-4894-a7b9-a9de53c57118)

Company: https://www.keypedia.com/companies/elos-medtech-skara-ab/81bbce1f-6f6d-41a8-a1e6-369490c7c854

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