FDA Inspection 925512 - Hoya Corporation - Pentax Life Division - April 21, 2015

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Record Details

This FDA Inspection record concerns Hoya Corporation - Pentax Life Division, with an inspection on April 21, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hoya Corporation - Pentax Life Division
Inspection Date: April 21, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 03769c88-4d36-4ddb-980b-4a0cc44e55ac

Violation Codes5

21 CFR 820.100(a)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.75(a)

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