FDA Inspection 885943 - Peter Lazic Gmbh - July 03, 2014

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Record Details

This FDA Inspection record concerns Peter Lazic Gmbh, with an inspection on July 3, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Peter Lazic Gmbh
Inspection Date: July 3, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d664dcf0-3b13-4e55-8858-25317a9a93e2

Violation Codes2

21 CFR 820.250(b)21 CFR 820.75(a)

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