FDA Inspection
Diasorin Inc.Diasorin Inc. – FDA Inspection, Sep 27, 2010
Record Details
This FDA Inspection record concerns Diasorin Inc., with an inspection on September 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Diasorin Inc.
- Inspection Date
- September 27, 2010
- Product Type
- Devices
View Company Profile
ID · 1ec7b054-6cfe-4ea0-ba3c-315bb5e41b58
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 680056
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 806.20(a)Records not kept
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Diasorin Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 13, 2026 | Not classified | Minneapolis District Office | |
| February 1, 2019 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| June 4, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Diasorin Inc.
- FDA Inspection 1301080 - 2026-01-13
- FDA Inspection 1081144 - 2019-02-01
- FDA Inspection 938219 - 2015-06-04
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