# FDA 483 - Iotamotion Inc - September 12, 2024

Source: https://www.keypedia.com/records/483/iotamotion-inc/c9281e46-0f18-4fdb-a634-df404cc3eea8

> FDA 483 for Iotamotion Inc on September 12, 2024. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Iotamotion Inc
- Inspection Date: 2024-09-12
- Product Type: device
- Office Name: Minneapolis District Office
- Summary: An FDA inspection of Iotamotion Inc, a medical device manufacturer in Vadnais Heights, MN, revealed a significant lapse in quality control. The firm failed to adequately examine labeling for accuracy before release, leading to the shipment of mislabeled medical devices. This indicates a breakdown in adherence to their own established work instructions for visual inspection.

## Related Officers

- [Lashawn M. Elam](https://www.keypedia.com/people/lashawn-m-elam/23bee423-c2f7-4977-bc32-2d4c40fc521f)
- [Clifford F. Long](https://www.keypedia.com/people/clifford-f-long/846e5a0c-cb7c-421c-86aa-be9fddfbaaba)

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

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d