# FDA Inspection 1102242 - Dynofit Inc. - September 18, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/dynofit-inc/953f4a4d-78d5-48e6-8be6-2ab4879bfece
Source feed: FDA_Inspections

> FDA Inspection 1102242 for Dynofit Inc. on September 18, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102242
- Company Name: Dynofit Inc.
- Inspection Date: 2019-09-18
- 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 1102242 - 2019-09-18](https://www.globalkeysolutions.net/records/fda_inspections/dynofit-inc/4e7b85ea-d0c8-4416-ba00-98cfcecb1413)

Company: https://www.globalkeysolutions.net/companies/dynofit-inc/afd3474d-52b0-4446-8b16-5a79dd65ebe0

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