FDA Inspection 926494 - HOYA Corporation PENTAX Miyagi Factory - April 24, 2015

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Record Details

This FDA Inspection record concerns HOYA Corporation PENTAX Miyagi Factory, with an inspection on April 24, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: HOYA Corporation PENTAX Miyagi Factory
Inspection Date: April 24, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4b45504d-40d1-413a-95e6-854ba344f150

Violation Codes3

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.75(a)

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