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FDA Inspection
•Vicon Motion Systems, Inc.•December 21, 2017

Vicon Motion Systems, Inc. – FDA Inspection, Dec 21, 2017

Record Details

This FDA Inspection record concerns Vicon Motion Systems, Inc., with an inspection on December 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Vicon Motion Systems, Inc.
Inspection Date
December 21, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Matthew M. Vernon (Company Rep)
View Company Profile

ID · 8c75d11c-f157-4c6e-a29e-c4449d4c567b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1038632
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Vicon Motion Systems, Inc.

2
DateClassificationOfficeProject area
June 11, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
September 22, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Vicon Motion Systems, Inc.
  • FDA Inspection 836303 - 2013-06-11
  • FDA Inspection 614966 - 2009-09-22

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