FDA inspection

Megadyne Medical Products, Inc.: FDA inspection ending Dec 10, 2009

FDA inspection 632644 · Voluntary Action Indicated (VAI) · Blue Ash, OH

Key facts

Inspection ID 632644
Firm Megadyne Medical Products, Inc.
FEI number 1721194
Address 11506 S State St
City Blue Ash
State OH
ZIP 45242
Country United States
Fiscal year 2010
Inspection end date Dec 10, 2009
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 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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