# FDA Inspection 970735 - PENTAX of America Inc - March 11, 2016

Source: https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/edb6b1d3-27a3-4239-9e37-369d47376204
Source feed: FDA_Inspections

> FDA Inspection 970735 for PENTAX of America Inc on March 11, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 970735
- Company Name: PENTAX of America Inc
- Inspection Date: 2016-03-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 970735 - 2016-03-11](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/58c551bc-7489-4326-9c56-30f8c2cd6b85)
- [FDA Inspection 888891 - 2014-07-28](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/d66541bf-2a84-4ae5-916b-d6640e77f644)

Company: https://www.keypedia.com/companies/pentax-of-america-inc/3e359876-57bc-4c4a-a000-888dc92eee49

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