FDA Inspection
MAXTER CATHETERSMAXTER CATHETERS – FDA Inspection, Jul 31, 2014
Record Details
This FDA Inspection record concerns MAXTER CATHETERS, with an inspection on July 31, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MAXTER CATHETERS
- Inspection Date
- July 31, 2014
- Product Type
- Devices
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ID · 957be67b-0a21-4e24-afad-88f61a6730e8
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 891089
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
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