# Elos Medtech Skara AB – FDA Inspection, Mar 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-skara-ab/e88cc382-923f-4894-a7b9-a9de53c57118
Source feed: FDA_Inspections

> FDA inspection 1047590 of Elos Medtech Skara AB, March 23, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1220692 - 2023-08-31

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

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