# FDA Inspection 969980 - Technomed Europe - April 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/technomed-europe/8858ed3c-f6c6-4f9f-8ad1-35412f139162
Source feed: FDA_Inspections

> FDA Inspection 969980 for Technomed Europe on April 21, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 969980
- Company Name: Technomed Europe
- Inspection Date: 2016-04-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 807101 - 2012-09-27](https://www.keypedia.com/records/fda_inspections/technomed-europe/1625c145-7b5b-4331-9cbc-6ecae2cf044b)
- [FDA Inspection 807101 - 2012-09-27](https://www.keypedia.com/records/fda_inspections/technomed-europe/6a839aaf-06d2-4210-8d0d-f6e525a066de)

Company: https://www.keypedia.com/companies/technomed-europe/aa97fb5c-7179-41fe-a0f9-3b0b819ce3a3

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