FDA inspection

Misonix, Inc.: FDA inspection ending May 19, 2017

FDA inspection 1017560 · No Action Indicated (NAI) · Farmingdale, NY

Key facts

Inspection ID 1017560
Firm Misonix, Inc.
FEI number 2435119
Address 11830 Canon Blvd Ste A
City Farmingdale
State NY
ZIP 11735
Country United States
Fiscal year 2017
Inspection end date May 19, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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