# FDA Inspection 955250 - Tecfen Medical - January 05, 2016

Source: https://www.keypedia.com/records/fda_inspections/tecfen-medical/7af7b9fa-ed2f-4a21-95f2-61e018c2bcf0
Source feed: FDA_Inspections

> FDA Inspection 955250 for Tecfen Medical on January 05, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 955250
- Company Name: Tecfen Medical
- Inspection Date: 2016-01-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/tecfen-medical/d2c7a84a-2bbf-48c2-b334-ea6915745302

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