# FDA 483 - Desco Industries, Inc. - November 07, 2024

Source: https://www.keypedia.com/records/483/desco-industries-inc/e6defff5-e7e6-4383-ae5a-0a2a29cdfbd1

> FDA 483 for Desco Industries, Inc. on November 07, 2024. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Desco Industries, Inc.
- Inspection Date: 2024-11-07
- Product Type: device
- Office Name: Los Angeles District Office
- Summary: An FDA inspection of Desco Industries, Inc., a contract manufacturer in Chino, CA, revealed a significant issue with their finished device acceptance procedures. The firm failed to adequately establish and follow procedures for reviewing and documenting dose audit records, which are critical for Device History Records. This indicates a lapse in quality system controls related to product release.

## Related Officers

- [Jordan I. Abel](https://www.keypedia.com/people/jordan-i-abel/9cdc8877-ab20-4c0c-a17e-a8534d4f13f2)
- [Marlo-Ian M. Alintanahin](https://www.keypedia.com/people/marlo-ian-m-alintanahin/a37da927-b369-4753-b275-41743556f25e)

Company: https://www.keypedia.com/companies/desco-industries-inc/dda4c29e-d030-4b6c-8b06-0f9ed4beec89

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b