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FDA Inspection
•Scantibodies Laboratory, Inc.•May 24, 2013

Scantibodies Laboratory, Inc. – FDA Inspection, May 24, 2013

Record Details

This FDA Inspection record concerns Scantibodies Laboratory, Inc., with an inspection on May 24, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Scantibodies Laboratory, Inc.
Inspection Date
May 24, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 478d5d42-6adb-4a43-8377-376990daaa07

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
829760
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Scantibodies Laboratory, Inc.

5
DateClassificationOfficeProject area
July 2, 2026Not classifiedLos Angeles District OfficeBlood and Blood Products
March 14, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
June 16, 2014VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 19, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 21, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Scantibodies Laboratory, Inc.
  • FDA Inspection 1325322 - 2026-07-02
  • FDA Inspection 1083561 - 2019-03-14
  • FDA Inspection 881586 - 2014-06-16
  • FDA Inspection 760535 - 2011-12-19
  • FDA Inspection 754602 - 2011-11-21

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