# FDA Inspection 906155 - Pentax of America Inc - December 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/853f56eb-10ea-4b19-bd7e-f630de314843
Source feed: FDA_Inspections

> FDA Inspection 906155 for Pentax of America Inc on December 17, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 906155
- Company Name: Pentax of America Inc
- Inspection Date: 2014-12-17
- 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.keypedia.com/companies/pentax-of-america-inc/4a00a7fe-b951-46eb-8a88-2842b89a05ad

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