FDA inspection

Intravena, LLC: FDA inspection ending Feb 17, 2011

FDA inspection 709989 · Voluntary Action Indicated (VAI) · Bountiful, UT

Key facts

Inspection ID 709989
Firm Intravena, LLC
FEI number 3007155346
Address 1898 Chokecherry Dr
City Bountiful
State UT
ZIP 84010
Country United States
Fiscal year 2011
Inspection end date Feb 17, 2011
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
  • 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