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FDA Inspection 925869 — Materialise USA LLC

Materialise USA LLC — FEI 3005718816

The FDA completed an inspection of Materialise USA LLC on May 12, 2015 in Plymouth, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Plymouth, MI (United States)

Facility

Other inspections at this facility

  • 1153886 (VAI Wed Oct 06 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022539 (NAI Tue Aug 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 858345 (NAI Tue Dec 10 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 720872 (VAI Fri Apr 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources