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FDA Inspection
•Medline Industries - Arlington Heights•December 6, 2017

Medline Industries - Arlington Heights – FDA Inspection, Dec 6, 2017

Record Details

This FDA Inspection record concerns Medline Industries - Arlington Heights, with an inspection on December 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Medline Industries - Arlington Heights
Inspection Date
December 6, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Todd Q. Dang (Issuing Officer)
View Company Profile

ID · a87ed627-a7eb-40aa-a55c-b64216b80d61

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1035723
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Medline Industries - Arlington Heights

5
DateClassificationOfficeProject area
February 6, 2026Not classifiedChicago District OfficeCompliance: Medical Devices
July 17, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 28, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
September 24, 2013OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 12, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Medline Industries - Arlington Heights
  • FDA Inspection 1299818 - 2026-02-06
  • FDA Inspection 936338 - 2015-07-17
  • FDA Inspection 881664 - 2014-05-28
  • FDA Inspection 846762 - 2013-09-24
  • FDA Inspection 666778 - 2010-05-12

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