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

Source: https://www.globalkeysolutions.net/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/f6f72b63-9d67-4914-b3f7-69825b6459f7/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 857579
- Company Name: HOYA Corporation PENTAX Miyagi Factory
- Inspection Date: 2013-11-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/hoya-corporation-pentax-miyagi-factory/581745ee-6ba6-4267-9528-b88f8c68388b

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7