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FDA Inspection 1083561 — Scantibodies Laboratory, Inc.

Scantibodies Laboratory, Inc. — FEI 2020808

The FDA completed an inspection of Scantibodies Laboratory, Inc. on March 14, 2019 in Santee, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 14, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Santee, CA (United States)

Facility

Other inspections at this facility

  • 881586 (VAI Mon Jun 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 829760 (OAI Fri May 24 2013 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