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FDA Inspection 955782 — Megadyne Medical Products, Inc.

Megadyne Medical Products, Inc. — FEI 1721194

The FDA completed an inspection of Megadyne Medical Products, Inc. on December 11, 2015 in Blue Ash, OH. 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
December 11, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Blue Ash, OH (United States)

Facility

Other inspections at this facility

  • 1256322 (NAI Fri Nov 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1208218 (NAI Tue Jun 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809350 (NAI Thu Dec 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 632644 (NAI Thu Dec 10 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources