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FDA Inspection
•Akers Biosciences, Inc.•May 9, 2011

Akers Biosciences, Inc. – FDA Inspection, May 9, 2011

Record Details

This FDA Inspection record concerns Akers Biosciences, Inc., with an inspection on May 9, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Akers Biosciences, Inc.
Inspection Date
May 9, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · f848ebf2-ab9e-401c-85b6-f68a49d47fc1

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
721635
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Akers Biosciences, Inc.

3
DateClassificationOfficeProject area
November 4, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
April 11, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
April 9, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Akers Biosciences, Inc.
  • FDA Inspection 947128 - 2015-11-04
  • FDA Inspection 775226 - 2012-04-11
  • FDA Inspection 571594 - 2009-04-09

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