# FDA Inspection 1070002 - Tecnimed S.R.L. - September 05, 2018

Source: https://www.keypedia.com/records/fda_inspections/tecnimed-srl/a8db67f0-c602-45e6-b93a-da568c3a396d
Source feed: FDA_Inspections

> FDA Inspection 1070002 for Tecnimed S.R.L. on September 05, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1070002
- Company Name: Tecnimed S.R.L.
- Inspection Date: 2018-09-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 759125 - 2011-11-30](https://www.keypedia.com/records/fda_inspections/tecnimed-srl/f1d113e0-84cd-49b3-8e70-a993278c613f)

Company: https://www.keypedia.com/companies/tecnimed-srl/c9776448-eddd-4160-a49a-31d3815071c6

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