# Meditech KFT – FDA Inspection, Jan 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/meditech-kft/3b147ba4-038c-4b41-9cd2-71f0cade36ce
Source feed: FDA_Inspections

> FDA inspection 921149 of Meditech KFT, January 15, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 921149
- Company Name: Meditech KFT
- Inspection Date: 2015-01-15
- 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: 2

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Company: https://www.keypedia.com/companies/meditech-kft/b98981ca-fdfa-4ba9-a8cf-ae68e104157f

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