# FDA Inspection 1078835 - ELOS MEDTECH PINOL A/S - February 07, 2019

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

> FDA Inspection 1078835 for ELOS MEDTECH PINOL A/S on February 07, 2019. Classification: Voluntary Action Indicated (VAI).

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## 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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 864555 - 2013-11-21](https://www.globalkeysolutions.net/records/fda_inspections/elos-medtech-pinol-as/e5d81bfb-c6db-4e87-a7ca-f5365b470419)
- [FDA Inspection 685840 - 2010-09-24](https://www.globalkeysolutions.net/records/fda_inspections/elos-medtech-pinol-as/eecbdd59-c372-42f9-ac7d-3dfa8723249f)

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

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