# FDA Inspection 938205 - SURESTEP, LLC - August 05, 2015

Source: https://www.keypedia.com/records/fda_inspections/surestep-llc/3f9ba325-f536-4447-832d-2486b54ecc45
Source feed: FDA_Inspections

> FDA Inspection 938205 for SURESTEP, LLC on August 05, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938205
- Company Name: SURESTEP, LLC
- Inspection Date: 2015-08-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/surestep-llc/e9c86e30-dfd1-4615-962a-014aff789377

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