FDA Inspection 1106963 - Perryman Company - October 10, 2019

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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 · 0821bfd0-f144-4973-ad29-348a807f4c54

Violation Codes2

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

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FDA Inspection

Perryman CompanyOctober 10, 2019