# FDA 483 - MD Labs, LLC - March 06, 2025

Source: https://www.globalkeysolutions.net/records/483/md-labs-llc/64bda8c6-74c7-4aa3-986a-9246d91d2715

> FDA 483 for MD Labs, LLC on March 06, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: MD Labs, LLC
- Inspection Date: 2025-03-06
- Product Type: device
- Office Name: Los Angeles District Office
- Summary: An FDA inspection of MD Labs, LLC, a medical device manufacturer in Westlake Village, CA, identified one significant observation. The firm failed to adequately maintain device history records, specifically by not including or referencing unique device identifiers (UDI) or universal product codes (UPC) as required by their own quality procedures.

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.globalkeysolutions.net/companies/md-labs-llc/d9f78f83-4fb2-4afc-a131-51dbcfd70e3a

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