FDA inspection

CURALLUX LLC: FDA inspection ending Nov 7, 2014

FDA inspection 900767 · Official Action Indicated (OAI) · Doral, FL

Key facts

Inspection ID 900767
Firm CURALLUX LLC
FEI number 3010123655
Address 1715 NW 82nd Ave
City Doral
State FL
ZIP 33126
Country United States
Fiscal year 2015
Inspection end date Nov 7, 2014
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices

At a glance

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