# FDA Inspection 1249533 - Iotamotion Inc - September 12, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/iotamotion-inc/33eb682f-7fd7-436f-8b2b-88058c4afd04
Source feed: FDA_Inspections

> FDA Inspection 1249533 for Iotamotion Inc on September 12, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1249533
- Company Name: Iotamotion Inc
- Inspection Date: 2024-09-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1249533 - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/iotamotion-inc/543d2863-a725-4785-a6b0-48c1da0cc566)
- [FDA Inspection 1249533 - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/iotamotion-inc/999f043a-128c-4cb8-b51d-de7eb6532c1a)
- [FDA Inspection 1249533 - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/iotamotion-inc/b1f51d93-42c3-47df-8c3f-c53cee4ada99)

Company: https://www.globalkeysolutions.net/companies/iotamotion-inc/9d7dea3c-109c-4947-a6bb-35963e1419a0

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