# Quidel Corporation – FDA Inspection, Jan 17, 2013

Source: https://www.keypedia.com/records/fda_inspections/quidel-corporation/6f0420c2-0af1-4bca-9e47-0c6ca666503e
Source feed: FDA_Inspections

> FDA inspection 816786 of Quidel Corporation, January 17, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816786
- Company Name: Quidel Corporation
- Inspection Date: 2013-01-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1149132 - 2021-08-03
- [FDA Inspection 1041292 - 2018-01-29](https://www.keypedia.com/records/fda_inspections/quidel-corporation/ff55cd9d-e991-42f6-af52-85cb4fd8c2c4)
- FDA Inspection 834600 - 2013-05-21
- FDA Inspection 715087 - 2011-03-16
- FDA Inspection 614117 - 2009-09-24

Company: https://www.keypedia.com/companies/quidel-corporation/a4399182-31b3-4c3e-9cee-eb0c4628baaa

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