# Coloplast Manufacturing US, LLC, Minneapolis, MN – FDA Inspections

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

> Inspection records and compliance data for Coloplast Manufacturing US, LLC in Minneapolis, Minnesota. 12 FDA inspections on record, 1 Form 483, last inspected March 06, 2026.

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## Details

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

## Related Documents

- FDA Inspection 1307530 - Coloplast Manufacturing US, LLC - 2026-03-06 — source: FDA, date: March 6, 2026
- FDA Inspection 1196697 - Coloplast Manufacturing US, LLC - 2023-01-20 — classification: No Action Indicated (NAI), source: FDA, date: January 20, 2023
- FDA Inspection 1196697 - Coloplast Manufacturing US, LLC - 2023-01-20 — classification: No Action Indicated (NAI), source: FDA, date: January 20, 2023
- FDA Inspection 1080994 - Coloplast Manufacturing US, LLC - 2019-02-06 — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2019
- FDA Inspection 1066755 - Coloplast Manufacturing US, LLC - 2018-09-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2018
- [FDA Inspection 1066755 - Coloplast Manufacturing US, LLC - 2018-09-25](https://www.keypedia.com/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 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2018
- FDA Inspection 1068220 - Coloplast Manufacturing US, LLC - 2018-09-14 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2018
- FDA Inspection 997753 - Coloplast Manufacturing US, LLC - 2016-11-09 — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2016
- FDA Inspection 997753 - Coloplast Manufacturing US, LLC - 2016-11-09 — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2016

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