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FDA Inspection
•Xeridiem Medical Devices, Inc.•February 7, 2020

Xeridiem Medical Devices, Inc. – FDA Inspection, Feb 7, 2020

Record Details

This FDA Inspection record concerns Xeridiem Medical Devices, Inc., with an inspection on February 7, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company
Xeridiem Medical Devices, Inc.
Inspection Date
February 7, 2020
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 50f830c6-7e2e-4a9f-9cbd-ea72f86c5b72

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1118179
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Xeridiem Medical Devices, Inc.

2
DateClassificationOfficeProject area
July 12, 2019Not classifiedDenver District Office
July 24, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Xeridiem Medical Devices, Inc.
  • FDA Inspection 1158152 - 2019-07-12
  • FDA Inspection 842401 - 2013-07-24

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