# FDA Inspection 1068220 - Coloplast Manufacturing US, LLC - September 14, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/coloplast-manufacturing-us-llc/fb5c9c52-ed39-4ee1-ad6a-24d1bcab7322/
Source feed: FDA_Inspections

> FDA Inspection 1068220 for Coloplast Manufacturing US, LLC on September 14, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1068220
- Company Name: Coloplast Manufacturing US, LLC
- Inspection Date: 2018-09-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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