FDA Inspection 1066901 - Pentax of America Inc - September 27, 2018

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Record Details

This FDA Inspection record concerns Pentax of America Inc, with an inspection on September 27, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Pentax of America Inc
Inspection Date: September 27, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 81484047-f062-4a03-9b73-085884f39ec1

Violation Codes5

21 CFR 803.17(a)(2)21 CFR 803.50(a)(1)21 CFR 803.50(a)(2)21 CFR 820.100(a)21 CFR 820.200(c)

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