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

Source: https://www.keypedia.com/records/fda_inspections/coloplast-hungary-kft/ac049e49-e674-438d-a951-f12a1d0169b4
Source feed: FDA_Inspections

> FDA inspection 607321 of Coloplast Hungary, KFT., June 25, 2009. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 607321
- Company Name: Coloplast Hungary, KFT.
- Inspection Date: 2009-06-25
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1024793 - 2017-09-01](https://www.keypedia.com/records/fda_inspections/coloplast-hungary-kft/3968832f-7351-4f40-8f41-e8567a3a462a)
- FDA Inspection 868322 - 2014-03-04

Company: https://www.keypedia.com/companies/coloplast-hungary-kft/cc7e69ef-1602-495c-9cde-ab007815919b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7