FDA Inspection 1033966 — Hardy Diagnostics

Hardy Diagnostics — FEI 3009547954

The FDA completed an inspection of Hardy Diagnostics on Nov 8, 2017 in Springboro, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 8, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Springboro, OH (United States)