FDA Inspection
Koko GmbHKoko GmbH – FDA Inspection, Feb 23, 2012
Record Details
This FDA Inspection record concerns Koko GmbH, with an inspection on February 23, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Koko GmbH
- Inspection Date
- February 23, 2012
- Product Type
- Devices
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ID · ebf3f1b5-63a8-4496-8668-769671f90cff
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 774232
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
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