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FDA Inspection
•Tricol Biomedical, Inc.•December 18, 2013

Tricol Biomedical, Inc. – FDA Inspection, Dec 18, 2013

Record Details

This FDA Inspection record concerns Tricol Biomedical, Inc., with an inspection on December 18, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Tricol Biomedical, Inc.
Inspection Date
December 18, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · b9bd098d-b056-4d50-85ec-45c591d1f846

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
858577
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Tricol Biomedical, Inc.

4
DateClassificationOfficeProject area
April 2, 2018VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 31, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 11, 2009VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 2, 2009VAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Tricol Biomedical, Inc.
  • FDA Inspection 1047031 - 2018-04-02
  • FDA Inspection 902739 - 2014-10-31
  • FDA Inspection 634610 - 2009-12-11
  • FDA Inspection 635785 - 2009-12-02

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