# FDA Inspection 981369 - Fit-Pro KFT (Ltd.) - July 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/fit-pro-kft-ltd/e909001e-17b2-4560-a6d2-0b27d4173ff0
Source feed: FDA_Inspections

> FDA Inspection 981369 for Fit-Pro KFT (Ltd.) on July 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981369
- Company Name: Fit-Pro KFT (Ltd.)
- Inspection Date: 2016-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/fit-pro-kft-ltd/e4485a28-9bba-4787-8908-7924c05166b6

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