FDA inspection

Quantum Devices, Inc.: FDA inspection ending Aug 29, 2007

FDA inspection 485443 · No Action Indicated (NAI) · Barneveld, WI

Key facts

Inspection ID 485443
Firm Quantum Devices, Inc.
FEI number 3004181270
Address 112 E Orbison St
City Barneveld
State WI
ZIP 53507-9338
Fiscal year 2007
Inspection end date Aug 29, 2007
Classification No Action Indicated (NAI)
Project area Compliance: Med 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
  • 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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