# FDA Inspection 807101 - Technomed Europe - September 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/technomed-europe/1625c145-7b5b-4331-9cbc-6ecae2cf044b
Source feed: FDA_Inspections

> FDA Inspection 807101 for Technomed Europe on September 27, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 807101
- Company Name: Technomed Europe
- Inspection Date: 2012-09-27
- 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/technomed-europe/aa97fb5c-7179-41fe-a0f9-3b0b819ce3a3

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