FDA Inspection
Ms Marketing Inc. (DBA) EZ Lite CruiserMs Marketing Inc. (DBA) EZ Lite Cruiser – FDA Inspection, Jan 17, 2020
Record Details
This FDA Inspection record concerns Ms Marketing Inc. (DBA) EZ Lite Cruiser, with an inspection on January 17, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 17, 2020
- Product Type
- Devices
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ID · 5b372cdf-6665-4506-bef8-e93e748eac5b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1122659
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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