FDA inspection

NeoCoil, LLC: FDA inspection ending Oct 2, 2015

FDA inspection 955058 · No Action Indicated (NAI) · Pewaukee, WI

Key facts

Inspection ID 955058
Firm NeoCoil, LLC
FEI number 3006369484
Address N27W23910 Paul Rd Ste A
City Pewaukee
State WI
ZIP 53072
Country United States
Fiscal year 2016
Inspection end date Oct 2, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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