FDA Inspection 783891 - AcuLux, Inc. - May 30, 2012

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Record Details

This FDA Inspection record concerns AcuLux, Inc., with an inspection on May 30, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: AcuLux, Inc.
Inspection Date: May 30, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9bdf2080-04b2-4a8c-87f6-0e298709ae5a

Violation Codes7

21 CFR 803.1721 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.200(b)21 CFR 820.2221 CFR 820.50(a)21 CFR 820.70(e)

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