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FDA Inspection
•Quidel Corporation•April 10, 2017

Quidel Corporation – FDA Inspection, Apr 10, 2017

Record Details

This FDA Inspection record concerns Quidel Corporation, with an inspection on April 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Quidel Corporation
Inspection Date
April 10, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Scott K. Zika (Issuing Officer)
View Company Profile

ID · e85f17c3-2b8f-47e0-bb00-a8330c456375

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1010641
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Quidel Corporation

2
DateClassificationOfficeProject area
July 27, 2018Not classifiedLos Angeles District Office
January 13, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Quidel Corporation
  • FDA Inspection 1135845 - 2018-07-27
  • FDA Inspection 861748 - 2014-01-13

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