# FDA Inspection 929019 - Coloplast A/S - March 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/coloplast-as/d1ef2354-0e92-40e1-b7b0-af48acd4e1b6
Source feed: FDA_Inspections

> FDA Inspection 929019 for Coloplast A/S on March 12, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 929019
- Company Name: Coloplast A/S
- Inspection Date: 2015-03-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 929019 - 2015-03-12](https://www.keypedia.com/records/fda_inspections/coloplast-as/28ec84c3-af82-479a-a949-06d7e6d1187d)

Company: https://www.keypedia.com/companies/coloplast-as/635b8af2-1476-4036-b6d9-c19302872a6d

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