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

Source: https://www.keypedia.com/records/fda_inspections/koko-llc/55815248-db2e-4fa1-8112-d3bb8b61baa9
Source feed: FDA_Inspections

> FDA inspection 1018309 of Koko, LLC, June 14, 2017. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1134958 - 2021-01-25
- FDA Inspection 853148 - 2013-10-28
- FDA Inspection 643636 - 2010-02-09

Company: https://www.keypedia.com/companies/koko-llc/06e25f74-f947-4553-82e3-351694ba93e8

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