# Coloplast Manufacturing US, LLC – FDA Inspection, Sep 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/coloplast-manufacturing-us-llc/b8c4626f-964e-4440-9cae-4f3f1e99c904
Source feed: FDA_Inspections

> FDA inspection 1066755 of Coloplast Manufacturing US, LLC, September 25, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 11 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066755
- Company Name: Coloplast Manufacturing US, LLC
- Inspection Date: 2018-09-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kellie-l-thommes/255a1b92-cd56-41f5-9622-82e8a629e153)

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