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

Source: https://www.globalkeysolutions.net/records/fda_inspections/hoya-pentax-corporation/fdb5d8d1-8fb6-4f84-8e68-d8a66c739f6f/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 890084
- Company Name: Hoya Pentax Corporation
- Inspection Date: 2014-07-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/hoya-pentax-corporation/f791f8be-2997-4376-b4bd-f61ac203b95f

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