FDA Inspection 840250 - STRATEC SE - June 06, 2013

Record Details

This FDA Inspection record concerns STRATEC SE, with an inspection on June 6, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: STRATEC SE
Inspection Date: June 6, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 2f272b05-f8f0-4f3c-b05f-4080835a65bf

Violation Codes2

21 CFR 820.100(a)21 CFR 820.250(b)

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