# Quidel Corporation – FDA Inspection, Apr 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/quidel-corporation/e85f17c3-2b8f-47e0-bb00-a8330c456375
Source feed: FDA_Inspections

> FDA inspection 1010641 of Quidel Corporation, April 10, 2017. Classification: No Action Indicated (NAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010641
- Company Name: Quidel Corporation
- Inspection Date: 2017-04-10
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1135845 - 2018-07-27](https://www.keypedia.com/records/fda_inspections/quidel-corporation/07079569-c675-41de-8770-d8956aa735c8)
- FDA Inspection 861748 - 2014-01-13

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/scott-k-zika/7f967edd-5151-438b-a0e7-dd1db8a227d1)

Company: https://www.keypedia.com/companies/quidel-corporation/0b10b4f7-9e5b-407d-85e1-6060f9d185eb

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7