# FDA 483 - Mission Systems Davenport Inc. - March 30, 2023

Source: https://www.keypedia.com/records/483/mission-systems-davenport-inc/e4b1324f-4f52-495a-af76-4a05ee704ef0

> FDA 483 for Mission Systems Davenport Inc. on March 30, 2023. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Mission Systems Davenport Inc.
- Inspection Date: 2023-03-30
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - West II
- Summary: An FDA inspection of Mission Systems Davenport Inc. in Davenport, IA, a medical device manufacturer, identified a significant compliance issue. The firm failed to include unique device identifiers (UDI) or universal product codes (UPC) in the device history record or on the labeling for their Class II AIRCRAFT MEDICAL OXYGEN GENERATION SYSTEM (AMOGS) Oxygen Concentrator. This indicates a deficiency in their device labeling and record-keeping practices.

## Related Officers

- [Clifford F. Long](https://www.keypedia.com/people/clifford-f-long/846e5a0c-cb7c-421c-86aa-be9fddfbaaba)

Company: https://www.keypedia.com/companies/mission-systems-davenport-inc/f438ec8f-3115-497d-b174-9d7140182cea

Office: https://www.keypedia.com/offices/division-of-human-and-animal-food-operations-west-ii/8851d151-0390-4d17-be66-fd86d12aa6b8