# FDA Inspection 981370 - FIT-PRO KFT LTD - July 19, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/fit-pro-kft-ltd/f6522de1-e62e-47c8-a6a5-d0ac9a3c633a/
Source feed: FDA_Inspections

> FDA Inspection 981370 for FIT-PRO KFT LTD on July 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981370
- Company Name: FIT-PRO KFT LTD
- Inspection Date: 2016-07-19
- 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 981370 - 2016-07-19](https://www.globalkeysolutions.net/api/records/fda_inspections/fit-pro-kft-ltd/d97708ab-09c0-4076-b3c2-97dcb53eadb9/)

Company: https://www.globalkeysolutions.net/companies/fit-pro-kft-ltd/269dd4e1-a08d-4a9a-a6eb-212ab86e3fed

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