# FDA Inspection 938722 - Lorenz Lifetech spa - July 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/lorenz-lifetech-spa/b76486a7-7bfc-4b43-9929-9fb13f1f9890
Source feed: FDA_Inspections

> FDA Inspection 938722 for Lorenz Lifetech spa on July 30, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938722
- Company Name: Lorenz Lifetech spa
- Inspection Date: 2015-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 938722 - 2015-07-30](https://www.keypedia.com/records/fda_inspections/lorenz-lifetech-spa/eba27bc9-a238-4477-8ea0-59cf15487e27)

Company: https://www.keypedia.com/companies/lorenz-lifetech-spa/e25ca706-d3ce-45bb-a498-990ed3223c03

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