# FDA Inspection 583525 - Pentax of America Inc - May 18, 2009

Source: https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/4b79121c-0ede-4e1e-9f7c-d587aea39504
Source feed: FDA_Inspections

> FDA Inspection 583525 for Pentax of America Inc on May 18, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 583525
- Company Name: Pentax of America Inc
- Inspection Date: 2009-05-18
- 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 1211451 - 2023-07-20](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/c2dbefbe-b82d-4d2f-ab20-89e179389e15)
- [FDA Inspection 1211451 - 2023-07-20](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/53261da2-3c50-44a6-ac3f-c20b05d82dd1)
- [FDA Inspection 1066901 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/44cb5503-c0af-42da-a482-915328ed8a80)
- [FDA Inspection 1066901 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/81484047-f062-4a03-9b73-085884f39ec1)
- [FDA Inspection 921077 - 2015-04-02](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/541ecc12-0352-4126-a88f-0e2a2febdc17)

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