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FDA Inspection
•Anchor Products Company, Inc.•June 4, 2010

Anchor Products Company, Inc. – FDA Inspection, Jun 4, 2010

Record Details

This FDA Inspection record concerns Anchor Products Company, Inc., with an inspection on June 4, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Anchor Products Company, Inc.
Inspection Date
June 4, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · fab3a09c-e8c0-4303-96a0-9f5c35e6e3d4

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
666324
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Anchor Products Company, Inc.

3
DateClassificationOfficeProject area
September 26, 2016NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 25, 2013VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 12, 2011VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Anchor Products Company, Inc.
  • FDA Inspection 985552 - 2016-09-26
  • FDA Inspection 854186 - 2013-10-25
  • FDA Inspection 725032 - 2011-05-12

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