FDA inspection

Hamilton Enterprises, Inc. / dba: Quintron Instrument Co.: FDA inspection ending Mar 12, 2020

FDA inspection 1147133 · Voluntary Action Indicated (VAI) · Milwaukee, WI

Key facts

Inspection ID 1147133
Firm Hamilton Enterprises, Inc. / dba: Quintron Instrument Co.
FEI number 2124914
Address 3712 W Pierce St
City Milwaukee
State WI
ZIP 53215-1032
Fiscal year 2020
Inspection end date Mar 12, 2020
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None 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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