# ELOS MEDTECH PINOL A/S – FDA Inspection, Sep 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-pinol-as/eecbdd59-c372-42f9-ac7d-3dfa8723249f
Source feed: FDA_Inspections

> FDA inspection 685840 of ELOS MEDTECH PINOL A/S, September 24, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 685840
- Company Name: ELOS MEDTECH PINOL A/S
- Inspection Date: 2010-09-24
- 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 1078835 - 2019-02-07](https://www.keypedia.com/records/fda_inspections/elos-medtech-pinol-as/878586b2-3b20-4aaa-a409-093570ca43f1)
- FDA Inspection 864555 - 2013-11-21

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