FDA Inspection
Quidel CorporationQuidel Corporation – FDA Inspection, Jan 17, 2013
Record Details
This FDA Inspection record concerns Quidel Corporation, with an inspection on January 17, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Quidel Corporation
- Inspection Date
- January 17, 2013
- Product Type
- Devices
View Company Profile
ID · 6f0420c2-0af1-4bca-9e47-0c6ca666503e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 816786
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.40(a)Not approved or obsolete document retrieval
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Quidel Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 3, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 29, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 21, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 16, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 24, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Quidel Corporation
- FDA Inspection 1149132 - 2021-08-03
- FDA Inspection 1041292 - 2018-01-29
- FDA Inspection 834600 - 2013-05-21
- FDA Inspection 715087 - 2011-03-16
- FDA Inspection 614117 - 2009-09-24
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