FDA Inspection
Tricor SystemsTricor Systems – FDA Inspection, Oct 9, 2008
Record Details
This FDA Inspection record concerns Tricor Systems, with an inspection on October 9, 2008, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Tricor Systems
- Inspection Date
- October 9, 2008
- Product Type
- Devices
View Company Profile
ID · dcf5819c-a7a1-4db4-b51e-ebba272d2f93
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 554108
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)Complete files maintained
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Tricor Systems
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 8, 2023 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 21, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 24, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Tricor Systems
- FDA Inspection 1199278 - 2023-03-08
- FDA Inspection 928462 - 2015-05-21
- FDA Inspection 711086 - 2011-02-24
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