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

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Record Details

This FDA Inspection record concerns Lorenz Lifetech spa, with an inspection on July 30, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Lorenz Lifetech spa
Inspection Date: July 30, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b76486a7-7bfc-4b43-9929-9fb13f1f9890

Violation Codes5

21 CFR 803.1721 CFR 820.30(e)21 CFR 820.30(g)21 CFR 820.30(h)21 CFR 820.80(b)

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