FDA inspection

NeoSoft, LLC: FDA inspection ending Mar 31, 2015

FDA inspection 920789 · Voluntary Action Indicated (VAI) · Pewaukee, WI

Key facts

Inspection ID 920789
Firm NeoSoft, LLC
FEI number 3005914761
Address N-27W23910B Paul Rd
City Pewaukee
State WI
ZIP 53072
Country United States
Fiscal year 2015
Inspection end date Mar 31, 2015
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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