FDA Inspection 1100191 - Kelyniam Global, Inc. - August 15, 2019

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Record Details

This FDA Inspection record concerns Kelyniam Global, Inc., with an inspection on August 15, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kelyniam Global, Inc.
Inspection Date: August 15, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8becbfdd-bdf2-469b-9329-849d3888b234

Violation Codes3

21 CFR 820.70(c)21 CFR 820.75(a)21 CFR 820.80(b)

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