FDA Inspection
HOYA Corporation PENTAX Miyagi FactoryFDA Inspection 705556 - HOYA Corporation PENTAX Miyagi Factory - December 16, 2010
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Record Details
This FDA Inspection record concerns HOYA Corporation PENTAX Miyagi Factory, with an inspection on December 16, 2010, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a64af382-d217-45a2-bce9-96829fe79523