# FDA 483 - MicroVision, Inc. - May 25, 2023

Source: https://www.keypedia.com/records/483/microvision-inc/dc537b49-29e5-4efe-8844-230c930de6a3

> FDA 483 for MicroVision, Inc. on May 25, 2023. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: MicroVision, Inc.
- Inspection Date: 2023-05-25
- Product Type: device
- Office Name: Division of Northeast Imports 
- Summary: An FDA inspection of MicroVision, Inc. in Seabrook, NH, a medical device manufacturer, identified significant deficiencies in its employee training procedures and documentation. The firm failed to adequately establish training needs and provide documented evidence of effective training. These issues led to multiple nonconformances and open CAPAs related to various operational procedures, indicating a systemic problem with ensuring employees are sufficiently trained for their manufacturing roles.

## Related Documents

- [483 - 2019-10-03](https://www.keypedia.com/records/483/microvision-inc/ab764b44-d35d-41b4-94da-31fad7e9a53e)

## Related Officers

- [Nadia R. Barreda](https://www.keypedia.com/people/nadia-r-barreda/ef624359-957a-45e4-89c9-5b5ff215c6aa)

Company: https://www.keypedia.com/companies/microvision-inc/fa83f1bb-e0a6-4450-a001-d97e2bb18200

Office: https://www.keypedia.com/offices/division-of-northeast-imports/b20599cf-9797-41fd-947f-6589ef596a94