# Laax, Inc. – FDA Inspection, 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 of Laax, Inc., May 22, 2015. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803, 806 and 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 814125 - 2013-01-15

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