# Coloplast Corp - Inspection Records

Source: https://www.keypedia.com/companies/coloplast-corp/c7749d8b-30c7-4836-9ff6-b933832244c3

> Inspection records and compliance data for Coloplast Corp in North Mankato, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Coloplast Corp
- FEI Number: 2125337
- City: North Mankato
- State: Minnesota
- Country Name: United States
- Address Line 1: 1940 Commerce Dr
- Zip Code: 56003

## Related Documents

- [483 - Coloplast Corp - 2024-04-11](https://www.keypedia.com/records/483/coloplast-corp/e97c16e6-72df-4a29-b416-f7562e784e36) — source: FDA, date: April 11, 2024
- [FDA Inspection 1236807 - Coloplast Corp - 2024-04-11](https://www.keypedia.com/records/fda_inspections/coloplast-corp/cefcac12-deae-4e04-b1da-3cfa19f02e93) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2024
- [FDA Inspection 921891 - Coloplast Corp - 2015-04-06](https://www.keypedia.com/records/fda_inspections/coloplast-corp/6270adf0-63c6-4388-b1fa-c5972c38118c) — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2015
- [FDA Inspection 921891 - Coloplast Corp - 2015-04-06](https://www.keypedia.com/records/fda_inspections/coloplast-corp/572e29ff-7ca8-4e91-96c0-f40c64ac8076) — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2015
- [FDA Inspection 791129 - Coloplast Corp - 2012-07-13](https://www.keypedia.com/records/fda_inspections/coloplast-corp/7c631a56-bc8a-4edb-b2ae-3f36d11143dc) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2012
- [FDA Inspection 653661 - Coloplast Corp - 2010-03-26](https://www.keypedia.com/records/fda_inspections/coloplast-corp/c4522491-9de1-4c50-bb7b-b948592d9b83) — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2010
- [FDA Inspection 653661 - Coloplast Corp - 2010-03-26](https://www.keypedia.com/records/fda_inspections/coloplast-corp/26332856-c174-4f92-840e-bc354eadb471) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 26, 2010

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