FDA Inspection 803393 - LISA Laser Products OHG - October 04, 2012

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Record Details

This FDA Inspection record concerns LISA Laser Products OHG, with an inspection on October 4, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: LISA Laser Products OHG
Inspection Date: October 4, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 14e7cb78-3ba9-4dec-b941-8edf58f02e6f

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(e)21 CFR 820.200(d)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(e)21 CFR 820.30(g)21 CFR 820.40(b)21 CFR 820.50

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