# FDA Inspection 1050339 - Sooka Inc - February 14, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/sooka-inc/0cbe7c18-10b2-4437-8d4e-7160f5e4d15b
Source feed: FDA_Inspections

> FDA Inspection 1050339 for Sooka Inc on February 14, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050339
- Company Name: Sooka Inc
- Inspection Date: 2018-02-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1050339 - 2018-02-14](https://www.globalkeysolutions.net/records/fda_inspections/sooka-inc/81a043cd-6f38-4f20-89a4-041398f63d73)
- [FDA Inspection 904633 - 2014-10-30](https://www.globalkeysolutions.net/records/fda_inspections/sooka-inc/2a84bf4c-4f28-4f66-b830-47cb22ab948a)
- [FDA Inspection 750866 - 2011-10-12](https://www.globalkeysolutions.net/records/fda_inspections/sooka-inc/dac32e89-0460-41ba-9c0d-8bc640e73bb0)

Company: https://www.globalkeysolutions.net/companies/sooka-inc/562592ad-3228-4287-a309-76a8d29b0f6c

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