# FDA Inspection 904880 - Tecan Austria GmbH - November 13, 2014

Source: https://www.keypedia.com/records/fda_inspections/tecan-austria-gmbh/cf6ce9ef-2092-4561-87d1-8e06ce491477
Source feed: FDA_Inspections

> FDA Inspection 904880 for Tecan Austria GmbH on November 13, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 904880
- Company Name: Tecan Austria GmbH
- Inspection Date: 2014-11-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 819145 - 2013-01-24](https://www.keypedia.com/records/fda_inspections/tecan-austria-gmbh/253ace84-6510-4d20-a63c-ff3d502c2836)
- [FDA Inspection 819145 - 2013-01-24](https://www.keypedia.com/records/fda_inspections/tecan-austria-gmbh/1f8b2d23-7896-4e57-b698-859543a080de)

Company: https://www.keypedia.com/companies/tecan-austria-gmbh/d854dc41-9693-4990-bce5-6dfa796879af

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