FDA Inspection 1064802 - Mannkind Corporation - September 07, 2018

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Record Details

This FDA Inspection record concerns Mannkind Corporation, with an inspection on September 7, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Mannkind Corporation
Inspection Date: September 7, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6a902049-a3d3-4fa6-a3c0-f4f6f7c61200

Violation Codes6

21 CFR 803.1721 CFR 803.50(a)(1)21 CFR 803.52(e)(4)21 CFR 820.184(f)21 CFR 820.198(a)21 CFR 820.30(g)

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