FDA Inspection 1248560 — Med Labs Inc

Med Labs Inc — FEI 2026803

The FDA completed an inspection of Med Labs Inc on Aug 20, 2024 in Goleta, 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
Aug 20, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Goleta, CA (United States)

Citations

IDCFRDescription
2279521 CFR 801.20(a)Label to bear a unique device identifier