# HOYA Corporation PENTAX Miyagi Factory – FDA Inspection, Dec 16, 2010

Source: https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/a64af382-d217-45a2-bce9-96829fe79523
Source feed: FDA_Inspections

> FDA inspection 705556 of HOYA Corporation PENTAX Miyagi Factory, December 16, 2010. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 705556
- Company Name: HOYA Corporation PENTAX Miyagi Factory
- Inspection Date: 2010-12-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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

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