FDA inspection

Cordis US Corp: FDA inspection ending Jul 6, 2016

FDA inspection 979906 · No Action Indicated (NAI) · Miami Lakes, FL

Key facts

Inspection ID 979906
Firm Cordis US Corp
FEI number 1016427
Address 1820 Mccarthy Blvd
City Miami Lakes
State FL
ZIP 33014
Country United States
Fiscal year 2016
Inspection end date Jul 6, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None 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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