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FDA Inspection
•Coloplast Hungary, KFT.•June 25, 2009

Coloplast Hungary, KFT. – FDA Inspection, Jun 25, 2009

Record Details

This FDA Inspection record concerns Coloplast Hungary, KFT., with an inspection on June 25, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Coloplast Hungary, KFT.
Inspection Date
June 25, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · ac049e49-e674-438d-a951-f12a1d0169b4

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
607321
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Coloplast Hungary, KFT.

2
DateClassificationOfficeProject area
September 1, 2017Not classifiedOffice of Inspections and InvestigationsCompliance: Devices
March 4, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Coloplast Hungary, KFT.
  • FDA Inspection 1024793 - 2017-09-01
  • FDA Inspection 868322 - 2014-03-04

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