# FDA Inspection 925512 - Hoya Corporation - Pentax Life Division - April 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-life-division/a75fb9ef-1742-4ce9-ae14-8d1d90d7281c
Source feed: FDA_Inspections

> FDA Inspection 925512 for Hoya Corporation - Pentax Life Division on April 21, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 925512
- Company Name: Hoya Corporation - Pentax Life Division
- Inspection Date: 2015-04-21
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 925512 - 2015-04-21](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-life-division/03769c88-4d36-4ddb-980b-4a0cc44e55ac)
- [FDA Inspection 890110 - 2014-07-15](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-life-division/1f0c2161-3446-4df4-99d2-1599fe2c884f)
- [FDA Inspection 890110 - 2014-07-15](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-life-division/a21538d2-f4ee-46da-8515-518639b3685b)

Company: https://www.keypedia.com/companies/hoya-corporation-pentax-life-division/67c8d69c-e284-4639-bd32-f0f95911dda2

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