# FDA Inspection 1019048 - Straumann USA LLC - July 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/straumann-usa-llc/3b04fde1-e490-42cb-b66c-ceaa9009e1d8
Source feed: FDA_Inspections

> FDA Inspection 1019048 for Straumann USA LLC on July 21, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019048
- Company Name: Straumann USA LLC
- Inspection Date: 2017-07-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/straumann-usa-llc/9a27e5b2-2d25-4a71-a1d2-0cfda8b41aa0

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