# FDA Inspection 926803 - Laax, Inc. - May 22, 2015

Source: https://www.keypedia.com/records/fda_inspections/laax-inc/e0b7726e-6ca7-42e9-9224-7b2c885694b0
Source feed: FDA_Inspections

> FDA Inspection 926803 for Laax, Inc. on May 22, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926803
- Company Name: Laax, Inc.
- Inspection Date: 2015-05-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 926803 - 2015-05-22](https://www.keypedia.com/records/fda_inspections/laax-inc/63e724fa-f9fa-405f-87a2-c6706d626613)
- [FDA Inspection 814125 - 2013-01-15](https://www.keypedia.com/records/fda_inspections/laax-inc/bb13758f-2964-4ef6-bb2a-4533fd55a95c)
- [FDA Inspection 814125 - 2013-01-15](https://www.keypedia.com/records/fda_inspections/laax-inc/ed319100-5832-43a8-bdae-264812fcc287)

Company: https://www.keypedia.com/companies/laax-inc/d5a15319-fc7a-454f-b8d3-78d57a21fd7c

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