# FDA Inspection 1029050 - FootMaxx Inc. - September 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/footmaxx-inc/49974e92-edfe-4a6d-b72e-5a0188df7e9c
Source feed: FDA_Inspections

> FDA Inspection 1029050 for FootMaxx Inc. on September 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029050
- Company Name: FootMaxx Inc.
- Inspection Date: 2017-09-19
- 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/footmaxx-inc/0f2a8b5e-0d75-4762-9637-f1eb4e54c336

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