FDA Inspection 1084042 - Prestige Ameritech - March 27, 2019

Record Details

This FDA Inspection record concerns Prestige Ameritech, with an inspection on March 27, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Prestige Ameritech
Inspection Date: March 27, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · f415cb7d-3868-41c0-963e-75a00094671d

Violation Codes2

21 CFR 803.17(a)(3)21 CFR 820.198(a)

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