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FDA Inspection
•Scantibodies Laboratory, Inc.•November 21, 2011

Scantibodies Laboratory, Inc. – FDA Inspection, Nov 21, 2011

Record Details

This FDA Inspection record concerns Scantibodies Laboratory, Inc., with an inspection on November 21, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Scantibodies Laboratory, Inc.
Inspection Date
November 21, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c0d73313-4259-466e-a0e7-5befcb7dc97f

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
754602
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

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
May 24, 2013OAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 19, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
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 829760 - 2013-05-24
  • FDA Inspection 760535 - 2011-12-19

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