FDA Inspection 1256493 - Medshift - December 13, 2024

Record Details

This FDA Inspection record concerns Medshift, with an inspection on December 13, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medshift
Inspection Date: December 13, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · cb6ff8a0-4db5-4bc9-b8e7-18608e748b2b

Violation Codes10

21 CFR 820.18121 CFR 820.18421 CFR 820.20(b)(3)(ii)21 CFR 820.25(b)21 CFR 820.30(a)21 CFR 820.50(a)(1)21 CFR 820.50(a)(3)21 CFR 820.50(b)21 CFR 820.75(a)21 CFR 820.80(b)

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