FDA inspection

Oxus, Inc.: FDA inspection ending Aug 1, 2011

FDA inspection 738375 · Voluntary Action Indicated (VAI) · Auburn Hills, MI

Key facts

Inspection ID 738375
Firm Oxus, Inc.
FEI number 3008841036
Address 2046 Brown Rd
City Auburn Hills
State MI
ZIP 48326
Country United States
Fiscal year 2011
Inspection end date Aug 1, 2011
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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

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