# FDA 483 - Custom Assemblies, Inc. - July 19, 2019

Source: https://www.globalkeysolutions.net/records/483/custom-assemblies-inc/06309fd1-512f-41e9-a8cf-d922efe88170

> FDA 483 for Custom Assemblies, Inc. on July 19, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Custom Assemblies, Inc.
- Inspection Date: 2019-07-19
- Product Type: device
- Office Name: Atlanta District Office
- Summary: Custom Assemblies, Inc. in Pine Level, NC, a medical device manufacturer, received a Form FDA 483 with three observations. The firm was cited for failing to adequately validate its bonding and quality control processes for tubing products. Additionally, the company did not submit required Medical Device Reports for leaking administration sets and lacked established procedures for finished device acceptance, specifically concerning sterilization validation.

## Related Documents

- [483 - 2017-07-31](https://www.globalkeysolutions.net/records/483/custom-assemblies-inc/0ded2461-6ef3-48f5-8f73-3fc1e78c40d7)
- [483 - 2022-10-06](https://www.globalkeysolutions.net/records/483/custom-assemblies-inc/1b9e71f9-f67b-4257-87f2-2621ceb0aee7)

## Related Officers

- [Nicholas Z. Lu](https://www.globalkeysolutions.net/people/nicholas-z-lu/17448aca-e316-424c-b7b2-88c8baffc359)
- [issuing_officer](https://www.globalkeysolutions.net/people/david-e-lowe/1a2492c2-4a81-4486-b3af-37f6b7b5216a)

Company: https://www.globalkeysolutions.net/companies/custom-assemblies-inc/22d6dc22-42d3-4a2c-93e0-1da2d7a26140

Office: https://www.globalkeysolutions.net/offices/atlanta-district-office/7586d99a-288e-49d1-8c3d-d88b7354b7a7