FDA inspection

Materialise USA LLC: FDA inspection ending May 12, 2015

FDA inspection 925869 · Voluntary Action Indicated (VAI) · Plymouth, MI

Key facts

Inspection ID 925869
Firm Materialise USA LLC
FEI number 3005718816
Address 44650 Helm Ct
City Plymouth
State MI
ZIP 48170
Country United States
Fiscal year 2015
Inspection end date May 12, 2015
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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