# FDA Inspection 1018309 - Koko, LLC - June 14, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/koko-llc/84e8bb0e-0654-4a31-808a-eb344b2aabb7
Source feed: FDA_Inspections

> FDA Inspection 1018309 for Koko, LLC on June 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018309
- Company Name: Koko, LLC
- Inspection Date: 2017-06-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1134958 - 2021-01-25](https://www.globalkeysolutions.net/records/fda_inspections/koko-llc/bc6bb651-b50f-410b-88ab-3a88c8e1742e)
- [FDA Inspection 1134958 - 2021-01-25](https://www.globalkeysolutions.net/records/fda_inspections/koko-llc/2c028c9b-3436-499d-9743-fa8c6afeac85)
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- [FDA Inspection 853148 - 2013-10-28](https://www.globalkeysolutions.net/records/fda_inspections/koko-llc/c5a21189-36cb-4af4-9393-cc54462b91ad)
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Company: https://www.globalkeysolutions.net/companies/koko-llc/06e25f74-f947-4553-82e3-351694ba93e8

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