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FDA Inspection
•Koko, LLC•October 28, 2013

FDA Inspection 853148 - Koko, LLC - October 28, 2013

Record Details

This FDA Inspection record concerns Koko, LLC, with an inspection on October 28, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Koko, LLC
Inspection Date
October 28, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · b8d09105-1f18-4878-8a44-d7e044ead062

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
853148
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Koko, LLC

3
DateClassificationOfficeProject area
January 25, 2021VAICenter for Devices and Radiological HealthCompliance: Devices
June 14, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
February 9, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Koko, LLC
  • FDA Inspection 1134958 - 2021-01-25
  • FDA Inspection 1018309 - 2017-06-14
  • FDA Inspection 643636 - 2010-02-09

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