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FDA Inspection 829760 — Scantibodies Laboratory, Inc.

Scantibodies Laboratory, Inc. — FEI 2020808

The FDA completed an inspection of Scantibodies Laboratory, Inc. on May 24, 2013 in Santee, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 24, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santee, CA (United States)

Facility

Other inspections at this facility

  • 1083561 (VAI Thu Mar 14 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 881586 (VAI Mon Jun 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 760535 (NAI Mon Dec 19 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 754602 (NAI Mon Nov 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources