# FDA Inspection 864555 - ELOS MEDTECH PINOL A/S - November 21, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/elos-medtech-pinol-as/e5d81bfb-c6db-4e87-a7ca-f5365b470419
Source feed: FDA_Inspections

> FDA Inspection 864555 for ELOS MEDTECH PINOL A/S on November 21, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 864555
- Company Name: ELOS MEDTECH PINOL A/S
- Inspection Date: 2013-11-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1078835 - 2019-02-07](https://www.globalkeysolutions.net/records/fda_inspections/elos-medtech-pinol-as/878586b2-3b20-4aaa-a409-093570ca43f1)
- [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