FDA Inspection 1106963 - Perryman Company - October 10, 2019

Record Details

This FDA Inspection record concerns Perryman Company, with an inspection on October 10, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Perryman Company
Inspection Date: October 10, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8efa677d-4e36-4947-84d8-112f9c581481

Violation Codes2

21 CFR 820.100(a)21 CFR 820.198(c)

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