# FDA Inspection 1018613 - DC ELEKTRONIK AB - February 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/dc-elektronik-ab/1e60bbcb-a2e3-4381-abf7-e151bec5a00c
Source feed: FDA_Inspections

> FDA Inspection 1018613 for DC ELEKTRONIK AB on February 08, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018613
- Company Name: DC ELEKTRONIK AB
- Inspection Date: 2017-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/dc-elektronik-ab/0c1e5f2c-ab7a-4c1c-84f5-8f3938b20d23

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