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FDA Inspection 1017560 — Misonix, Inc.

Misonix, Inc. — FEI 2435119

The FDA completed an inspection of Misonix, Inc. on May 19, 2017 in Farmingdale, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 19, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Farmingdale, NY (United States)

Facility

Other inspections at this facility

  • 952742 (VAI Mon Dec 14 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 898643 (VAI Fri Oct 10 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 781232 (NAI Thu Apr 26 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 657067 (VAI Thu Mar 25 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources