# FDA Inspection 701343 - Eltech s.r.l. - December 09, 2010

Source: https://www.keypedia.com/records/fda_inspections/eltech-srl/67a842cb-17cd-4b86-877d-9c1f36da071c
Source feed: FDA_Inspections

> FDA Inspection 701343 for Eltech s.r.l. on December 09, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 701343
- Company Name: Eltech s.r.l.
- Inspection Date: 2010-12-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 894884 - 2014-08-29](https://www.keypedia.com/records/fda_inspections/eltech-srl/82be19e0-6e52-429d-92e4-8cdeb9180868)
- [FDA Inspection 701343 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/eltech-srl/a4a40cd9-f97c-4053-b899-f118f3a88fd9)

Company: https://www.keypedia.com/companies/eltech-srl/4d6ef59d-8e3f-49e1-a3d7-a8c8cad97362

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