# FDA Inspection 1010641 - Quidel Corporation - April 10, 2017

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

> FDA Inspection 1010641 for Quidel Corporation on April 10, 2017. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1010641 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/quidel-corporation/a845075d-30e0-4761-a8d5-332060f772c2)
- [FDA Inspection 861748 - 2014-01-13](https://www.keypedia.com/records/fda_inspections/quidel-corporation/8349618b-c7b1-4fc8-bc72-3737e6537a28)

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