# FDA Inspection 868322 - Coloplast Hungary, KFT. - March 04, 2014

Source: https://www.keypedia.com/records/fda_inspections/coloplast-hungary-kft/b197751c-3b0c-448a-a553-1feee0242007
Source feed: FDA_Inspections

> FDA Inspection 868322 for Coloplast Hungary, KFT. on March 04, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 868322
- Company Name: Coloplast Hungary, KFT.
- Inspection Date: 2014-03-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 868322 - 2014-03-04](https://www.keypedia.com/records/fda_inspections/coloplast-hungary-kft/6f9cb4a1-f9c4-4c01-ba5d-41752b07249b)
- [FDA Inspection 607321 - 2009-06-25](https://www.keypedia.com/records/fda_inspections/coloplast-hungary-kft/ac049e49-e674-438d-a951-f12a1d0169b4)

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