FDA Inspection 857579 - HOYA Corporation PENTAX Miyagi Factory - November 21, 2013

FDA Inspection 857579 for HOYA Corporation PENTAX Miyagi Factory on November 21, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 857579 for HOYA Corporation PENTAX Miyagi Factory on November 21, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.40

21 CFR 820.70(e)

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Record Information

Company

HOYA Corporation PENTAX Miyagi Factory

Inspection Date

November 21, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6f72b63-9d67-4914-b3f7-69825b6459f7

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