FDA Inspection 861748 — Quidel Corporation

Quidel Corporation — FEI 2024674

The FDA completed an inspection of Quidel Corporation on January 13, 2014 in San Diego, 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
January 13, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)