FDA inspection

Pure Source, LLC: FDA inspection ending Jul 28, 2026

FDA inspection 1328392 · Voluntary Action Indicated (VAI) · Doral, FL

Key facts

Inspection ID 1328392
Firm Pure Source, LLC
FEI number 3002754162
City Doral
State FL
ZIP 33172
Country United States
Fiscal year 2026
Inspection end date Jul 28, 2026
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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