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FDA Inspection
•Gambro Lundia AB•January 26, 2017

Gambro Lundia AB – FDA Inspection, Jan 26, 2017

Record Details

This FDA Inspection record concerns Gambro Lundia AB, with an inspection on January 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Gambro Lundia AB
Inspection Date
January 26, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • James R. Montero (Issuing Officer)
View Company Profile

ID · c9e726c8-a990-400b-88d7-dbe6076a24bd

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1002325
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Gambro Lundia AB

2
DateClassificationOfficeProject area
December 18, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
March 5, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Gambro Lundia AB
  • FDA Inspection 907494 - 2014-12-18
  • FDA Inspection 568201 - 2009-03-05

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