# Coloplast Manufacturing US, LLC – FDA Inspection, Sep 28, 2011

Source: https://www.keypedia.com/records/fda_inspections/coloplast-manufacturing-us-llc/475b00d7-580d-455d-bda5-99543e58b16d
Source feed: FDA_Inspections

> FDA inspection 744306 of Coloplast Manufacturing US, LLC, September 28, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 11 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 744306
- Company Name: Coloplast Manufacturing US, LLC
- Inspection Date: 2011-09-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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- [FDA Inspection 1066755 - 2018-09-25](https://www.keypedia.com/records/fda_inspections/coloplast-manufacturing-us-llc/b8c4626f-964e-4440-9cae-4f3f1e99c904)
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Company: https://www.keypedia.com/companies/coloplast-manufacturing-us-llc/fbedee38-0734-4861-b976-f0edc069d101

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