# DC ELEKTRONIK AB – FDA Inspection, Feb 8, 2017

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

> FDA inspection 1018613 of DC ELEKTRONIK AB, February 08, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1018613
- Company Name: DC ELEKTRONIK AB
- Inspection Date: 2017-02-08
- 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: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/yehualashet-a-gessesse/cb732900-358c-4982-a912-e98fa45142fe)

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