# FDA Inspection 818707 - Beautyko LLC - February 14, 2013

Source: https://www.keypedia.com/records/fda_inspections/beautyko-llc/7fbc72c6-f6af-4d89-903e-ede0bc6309dc
Source feed: FDA_Inspections

> FDA Inspection 818707 for Beautyko LLC on February 14, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 818707
- Company Name: Beautyko LLC
- Inspection Date: 2013-02-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 938660 - 2015-08-14](https://www.keypedia.com/records/fda_inspections/beautyko-llc/e543940a-83a4-4509-8101-f8f974404a13)

Company: https://www.keypedia.com/companies/beautyko-llc/7c299c18-0b80-41bf-bb32-fe6ea92cf412

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