# FDA Inspection 820749 - Eurogentec - January 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/eurogentec/b240cd6b-151a-49bd-894d-d9e70e5bee00
Source feed: FDA_Inspections

> FDA Inspection 820749 for Eurogentec on January 28, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820749
- Company Name: Eurogentec
- Inspection Date: 2013-01-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/eurogentec/1f28803f-bb85-4bff-9fd9-4d3676911282

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