FDA Inspection 750308 - KLS Martin SE & Co. KG - September 28, 2011

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Record Details

This FDA Inspection record concerns KLS Martin SE & Co. KG, with an inspection on September 28, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company: KLS Martin SE & Co. KG
Inspection Date: September 28, 2011
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5a2214d9-cda4-44c1-b160-d53610b02520

Violation Codes3

21 CFR 820.100(b)21 CFR 820.198(d)21 CFR 820.90(a)

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