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FDA Inspection
•Koko, LLC•June 14, 2017

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

Record Details

This FDA Inspection record concerns Koko, LLC, with an inspection on June 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Koko, LLC
Inspection Date
June 14, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 55815248-db2e-4fa1-8112-d3bb8b61baa9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1018309
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Koko, LLC

3
DateClassificationOfficeProject area
January 25, 2021VAICenter for Devices and Radiological HealthCompliance: Devices
October 28, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 9, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Koko, LLC
  • FDA Inspection 1134958 - 2021-01-25
  • FDA Inspection 853148 - 2013-10-28
  • FDA Inspection 643636 - 2010-02-09

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