# 3Shape Poland – FDA Inspection, Sep 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/3shape-poland/6d937e5f-274e-414a-94c6-02f050dec43b
Source feed: FDA_Inspections

> FDA inspection 851801 of 3Shape Poland, September 26, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1016400 - 2017-06-30](https://www.keypedia.com/records/fda_inspections/3shape-poland/5e6f5b58-2e9c-4d07-80f9-985f280f372d)

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