FDA Inspection 1149132 — Quidel Corporation

Quidel Corporation — FEI 1000122536

The FDA completed an inspection of Quidel Corporation on August 3, 2021 in Athens, OH. 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
August 3, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Athens, OH (United States)