# Coloplast Manufacturing US, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/coloplast-manufacturing-us-llc/fbedee38-0734-4861-b976-f0edc069d101

> Inspection records and compliance data for Coloplast Manufacturing US, LLC in Minneapolis, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Coloplast Manufacturing US, LLC
- FEI Number: 2125050
- City: Minneapolis
- State: Minnesota
- Country Name: United States
- Address Line 1: 1601 W River Rd
- Zip Code: 55411

## Related Documents

- [FDA Inspection 1307530 - Coloplast Manufacturing US, LLC - 2026-03-06](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/6af64fa6-a140-4a07-bb92-c93eea8dc8ef) — source: FDA, date: March 6, 2026
- [FDA Inspection 1196697 - Coloplast Manufacturing US, LLC - 2023-01-20](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/844371f3-f8b7-403c-92c6-afeb49f6a7f6) — classification: No Action Indicated (NAI), source: FDA, date: January 20, 2023
- [FDA Inspection 1196697 - Coloplast Manufacturing US, LLC - 2023-01-20](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/208841f8-db13-4880-af83-0a14849c9ac9) — classification: No Action Indicated (NAI), source: FDA, date: January 20, 2023
- [FDA Inspection 1080994 - Coloplast Manufacturing US, LLC - 2019-02-06](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/a24e73ad-f269-4bbe-9c32-59b336d3fc98) — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2019
- [FDA Inspection 1066755 - Coloplast Manufacturing US, LLC - 2018-09-25](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/b8c4626f-964e-4440-9cae-4f3f1e99c904) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2018
- [FDA Inspection 1068220 - Coloplast Manufacturing US, LLC - 2018-09-14](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/ba4a122b-4bd3-4cc0-b822-8d0561902779) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2018
- [FDA Inspection 1068220 - Coloplast Manufacturing US, LLC - 2018-09-14](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/fb5c9c52-ed39-4ee1-ad6a-24d1bcab7322) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2018
- [FDA Inspection 997753 - Coloplast Manufacturing US, LLC - 2016-11-09](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/4c918340-846c-448e-acdb-71ec29615422) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2016
- [FDA Inspection 997753 - Coloplast Manufacturing US, LLC - 2016-11-09](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/81f4eb23-1790-4033-beb3-81eae4e8897b) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2016
- [FDA Inspection 951146 - Coloplast Manufacturing US, LLC - 2015-11-24](https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/1a2c031d-0b84-4081-942e-6d841fe51d2d) — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015

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