# Meditech KFT – FDA Inspection, Apr 13, 2012

Source: https://www.keypedia.com/records/fda_inspections/meditech-kft/cd807e28-e4e5-4cf9-af33-bb2dbe368cac
Source feed: FDA_Inspections

> FDA inspection 779843 of Meditech KFT, April 13, 2012. Classification: Official Action Indicated (OAI). 9 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: 779843
- Company Name: Meditech KFT
- Inspection Date: 2012-04-13
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- [FDA Inspection 1057201 - 2018-06-28](https://www.keypedia.com/records/fda_inspections/meditech-kft/44db7653-9dcc-4bdd-8a4d-d43459171bea)
- [FDA Inspection 921149 - 2015-01-15](https://www.keypedia.com/records/fda_inspections/meditech-kft/3b147ba4-038c-4b41-9cd2-71f0cade36ce)

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
