FDA inspection

Megadyne Medical Products, Inc.: FDA inspection ending Jun 6, 2023

FDA inspection 1208218 · No Action Indicated (NAI) · Blue Ash, OH

Key facts

Inspection ID 1208218
Firm Megadyne Medical Products, Inc.
FEI number 1721194
Address 4545 Creek Rd
City Blue Ash
State OH
ZIP 45242
Country United States
Fiscal year 2023
Inspection end date Jun 6, 2023
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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