# ELOS MEDTECH PINOL A/S – FDA Inspection, Feb 7, 2019

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-pinol-as/878586b2-3b20-4aaa-a409-093570ca43f1
Source feed: FDA_Inspections

> FDA inspection 1078835 of ELOS MEDTECH PINOL A/S, February 07, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1078835
- Company Name: ELOS MEDTECH PINOL A/S
- Inspection Date: 2019-02-07
- 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: 2

## Related Documents

- FDA Inspection 864555 - 2013-11-21
- [FDA Inspection 685840 - 2010-09-24](https://www.keypedia.com/records/fda_inspections/elos-medtech-pinol-as/eecbdd59-c372-42f9-ac7d-3dfa8723249f)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/elos-medtech-pinol-as/78979286-b8b4-47cc-80d1-7ff458c794b3

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