FDA Inspection 1216969 — Pure Source, LLC

Pure Source, LLC — FEI 3002754162

The FDA completed an inspection of Pure Source, LLC on Aug 31, 2023 in Doral, FL. 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 31, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Doral, FL (United States)

Citations

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.