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FDA Inspection 1087820 — ARUP Laboratories Inc.

ARUP Laboratories Inc. — FEI 3008974012

The FDA completed an inspection of ARUP Laboratories Inc. on March 14, 2019 in Salt Lake City, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 14, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Salt Lake City, UT (United States)

Facility

Other inspections at this facility

  • 1244030 (NAI Thu Jun 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998808 (NAI Fri Dec 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 914102 (NAI Fri Feb 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 820206 (VAI Fri Feb 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756124 (VAI Fri Nov 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources