FDA Inspection 1216969 — Pure Source, LLC

Pure Source, LLC — FEI 3002754162

The FDA completed an inspection of Pure Source, LLC on August 31, 2023 in Doral, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 31, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Doral, FL (United States)

Citations

IDCFRDescription
342621 CFR 820.50(a)(1)Documented evaluation