# FDA Inspection 1056630 - Biocomposites GmbH (Former ARTOSS GmbH) - April 26, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/biocomposites-gmbh-former-artoss-gmbh/4a3b07d1-a93b-40b5-90e9-8e90205d192c
Source feed: FDA_Inspections

> FDA Inspection 1056630 for Biocomposites GmbH (Former ARTOSS GmbH) on April 26, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056630
- Company Name: Biocomposites GmbH (Former ARTOSS GmbH)
- Inspection Date: 2018-04-26
- 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/biocomposites-gmbh-former-artoss-gmbh/de40771b-9ed7-40d7-8df2-78672f6d74ea

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