FDA Inspection 1074037 — Hardy Diagnostics

Hardy Diagnostics — FEI 2022807

The FDA completed an inspection of Hardy Diagnostics on November 28, 2018 in Santa Maria, CA. 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
November 28, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Maria, CA (United States)