# FDA Inspection 851801 - 3Shape Poland - September 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/3shape-poland/6d781a7f-a735-41cc-9643-d43eea89e615
Source feed: FDA_Inspections

> FDA Inspection 851801 for 3Shape Poland on September 26, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 851801
- Company Name: 3Shape Poland
- Inspection Date: 2013-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 851801 - 2013-09-26](https://www.keypedia.com/records/fda_inspections/3shape-poland/6d937e5f-274e-414a-94c6-02f050dec43b)

Company: https://www.keypedia.com/companies/3shape-poland/9fa04a3a-2a78-4b83-8ab3-64833cfa8744

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