Home / Inspections / 614117

FDA Inspection 614117 — Quidel Corporation

Quidel Corporation — FEI 1000122536

The FDA completed an inspection of Quidel Corporation on September 24, 2009 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
September 24, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Athens, OH (United States)

Facility

Other inspections at this facility

  • 1149132 (NAI Tue Aug 03 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1041292 (VAI Mon Jan 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 834600 (NAI Tue May 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 816786 (VAI Thu Jan 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 715087 (NAI Wed Mar 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources