FDA Inspection 1262940 — MD Labs, LLC

MD Labs, LLC — FEI 3027686087

The FDA completed an inspection of MD Labs, LLC on Mar 6, 2025 in Westlake Village, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 6, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Westlake Village, CA (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained