# Eltech s.r.l. – FDA Inspection, Dec 9, 2010

Source: https://www.keypedia.com/records/fda_inspections/eltech-srl/a4a40cd9-f97c-4053-b899-f118f3a88fd9
Source feed: FDA_Inspections

> FDA inspection 701343 of Eltech s.r.l., December 09, 2010. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 701343
- Company Name: Eltech s.r.l.
- Inspection Date: 2010-12-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 894884 - 2014-08-29](https://www.keypedia.com/records/fda_inspections/eltech-srl/82be19e0-6e52-429d-92e4-8cdeb9180868)

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