# FDA Inspection 1057201 - Meditech KFT - June 28, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/meditech-kft/37386108-5fa1-43c8-96f5-f9eb26247289
Source feed: FDA_Inspections

> FDA Inspection 1057201 for Meditech KFT on June 28, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057201
- Company Name: Meditech KFT
- Inspection Date: 2018-06-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1057201 - 2018-06-28](https://www.globalkeysolutions.net/records/fda_inspections/meditech-kft/44db7653-9dcc-4bdd-8a4d-d43459171bea)
- [FDA Inspection 921149 - 2015-01-15](https://www.globalkeysolutions.net/records/fda_inspections/meditech-kft/3b147ba4-038c-4b41-9cd2-71f0cade36ce)
- [FDA Inspection 779843 - 2012-04-13](https://www.globalkeysolutions.net/records/fda_inspections/meditech-kft/cd807e28-e4e5-4cf9-af33-bb2dbe368cac)

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

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