# Elltec Co., Ltd. – FDA Inspection, Aug 12, 2010

Source: https://www.keypedia.com/records/fda_inspections/elltec-co-ltd/ed9c9a9c-51d3-4106-a6a5-42d7ab27d831
Source feed: FDA_Inspections

> FDA inspection 679349 of Elltec Co., Ltd., August 12, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 679349
- Company Name: Elltec Co., Ltd.
- Inspection Date: 2010-08-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

Company: https://www.keypedia.com/companies/elltec-co-ltd/2bfb2bee-947b-44e0-a7d3-18cbcce5dadc

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