FDA Inspection 956396 — Paragon Medical - Dayton

Paragon Medical - Dayton — FEI 1000200989

The FDA completed an inspection of Paragon Medical - Dayton on Jan 11, 2016 in Dayton, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 11, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dayton, OH (United States)