FDA Inspection
Scantibodies Laboratory, Inc.Scantibodies Laboratory, Inc. – FDA Inspection, Mar 14, 2019
Record Details
This FDA Inspection record concerns Scantibodies Laboratory, Inc., with an inspection on March 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 503380fa-fe8f-4ae9-9e72-a2765ca6c1ab
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1083561
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Scantibodies Laboratory, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| July 2, 2026 | Not classified | Los Angeles District Office | Blood and Blood Products |
| June 16, 2014 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 24, 2013 | OAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 19, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 21, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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