FDA Inspection 1010961 - Peter Kosek - April 21, 2017

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Record Details

This FDA Inspection record concerns Peter Kosek, with an inspection on April 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Peter Kosek
Inspection Date: April 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 14cedfb9-1119-404b-878c-7006f37bbf6b

Violation Codes3

21 CFR 50.25(a)(1)21 CFR 50.25(a)(2)21 CFR 50.25(a)(8)

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