FDA Inspection 632644 — Megadyne Medical Products, Inc.

Megadyne Medical Products, Inc. — FEI 1721194

The FDA completed an inspection of Megadyne Medical Products, Inc. on December 10, 2009 in Blue Ash, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 10, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Blue Ash, OH (United States)

Citations

IDCFRDescription
418921 CFR 820.198(a)General