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FDA Inspection
•Madison Polymeric Engineering•October 3, 2017

Madison Polymeric Engineering – FDA Inspection, Oct 3, 2017

Record Details

This FDA Inspection record concerns Madison Polymeric Engineering, with an inspection on October 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Madison Polymeric Engineering
Inspection Date
October 3, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Michael G. Mayfield (Company Rep)
View Company Profile

ID · 1656d2eb-843b-4231-8167-e656056173e8

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1027764
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Madison Polymeric Engineering

5
DateClassificationOfficeProject area
February 22, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
April 12, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
March 23, 2015OAICenter for Devices and Radiological HealthCompliance: Devices
January 9, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 26, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Madison Polymeric Engineering
  • FDA Inspection 1080354 - 2019-02-22
  • FDA Inspection 966463 - 2016-04-12
  • FDA Inspection 919396 - 2015-03-23
  • FDA Inspection 910590 - 2015-01-09
  • FDA Inspection 753106 - 2011-10-26

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