FDA Inspection
Tricol Biomedical, Inc.Tricol Biomedical, Inc. – FDA Inspection, Dec 2, 2009
Record Details
This FDA Inspection record concerns Tricol Biomedical, Inc., with an inspection on December 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Tricol Biomedical, Inc.
- Inspection Date
- December 2, 2009
- Product Type
- Devices
View Company Profile
ID · 75adb999-3f3b-4479-af30-f324e66d4f70
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 635785
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.40Sponsors" general responsibilities
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Tricol Biomedical, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 2, 2018 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 31, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 18, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 11, 2009 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Tricol Biomedical, Inc.
- FDA Inspection 1047031 - 2018-04-02
- FDA Inspection 902739 - 2014-10-31
- FDA Inspection 858577 - 2013-12-18
- FDA Inspection 634610 - 2009-12-11
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