FDA Inspection 890084 - Hoya Pentax Corporation - July 18, 2014

FDA Inspection 890084 for Hoya Pentax Corporation on July 18, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 890084 for Hoya Pentax Corporation on July 18, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

Hoya Pentax Corporation

Inspection Date

July 18, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdb5d8d1-8fb6-4f84-8e68-d8a66c739f6f

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