FDA inspection

Isolux, LLC: FDA inspection ending Nov 6, 2015

FDA inspection 948806 · Official Action Indicated (OAI) · Chatsworth, CA

Key facts

Inspection ID 948806
Firm Isolux, LLC
FEI number 3002249830
Address 1045 Collier Center Way Ste 7
City Chatsworth
State CA
ZIP 91311
Country United States
Fiscal year 2016
Inspection end date Nov 6, 2015
Classification Official Action Indicated (OAI)
Project area Postmarket Assurance: Devices
Product type Devices
Warning letter 486738

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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

Browse all FDA inspections