FDA Inspection 1063422 - Prestige Ameritech - August 20, 2018

Record Details

This FDA Inspection record concerns Prestige Ameritech, with an inspection on August 20, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Prestige Ameritech
Inspection Date: August 20, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b80b56b7-91b7-45e3-b248-254ab2cf5ce0

Violation Codes2

21 CFR 820.198(a)21 CFR 820.90(a)

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