# Lorenz Lifetech spa – FDA Inspection, Jul 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/lorenz-lifetech-spa/eba27bc9-a238-4477-8ea0-59cf15487e27
Source feed: FDA_Inspections

> FDA inspection 938722 of Lorenz Lifetech spa, July 30, 2015. Classification: Official Action Indicated (OAI). 5 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938722
- Company Name: Lorenz Lifetech spa
- Inspection Date: 2015-07-30
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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