# FDA Inspection 963535 - Soken Products, Inc - February 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/soken-products-inc/0b3d894e-5362-4eb4-bcf4-d21ee7de5e1f
Source feed: FDA_Inspections

> FDA Inspection 963535 for Soken Products, Inc on February 23, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 963535
- Company Name: Soken Products, Inc
- Inspection Date: 2016-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 581862 - 2009-05-13](https://www.keypedia.com/records/fda_inspections/soken-products-inc/cd0d1cbf-a5ad-481f-b961-aed9bc32f0dc)
- [FDA Inspection 581862 - 2009-05-13](https://www.keypedia.com/records/fda_inspections/soken-products-inc/c0b7b316-2048-407e-af67-5b802b8ebf2a)

Company: https://www.keypedia.com/companies/soken-products-inc/7b74c4ce-a7d5-4f50-849e-ce036582991a

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