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FDA Inspection
•FreeRider Corporation•September 21, 2017

FreeRider Corporation – FDA Inspection, Sep 21, 2017

Record Details

This FDA Inspection record concerns FreeRider Corporation, with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
FreeRider Corporation
Inspection Date
September 21, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Jeffrey J. Thibodeau (FDA Associated Person)
View Company Profile

ID · 6406bbbf-6bdc-4020-a62b-b5bf9c20605f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1029727
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of FreeRider Corporation

2
DateClassificationOfficeProject area
January 14, 2026NAICompliance: Devices
March 19, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for FreeRider Corporation
  • FDA Inspection 1302594 - 2026-01-14
  • FDA Inspection 873838 - 2014-03-19

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