FDA Inspection 998801 — ARUP Laboratories, Inc.

ARUP Laboratories, Inc. — FEI 3004741920

The FDA completed an inspection of ARUP Laboratories, Inc. on November 18, 2016 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 18, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Salt Lake City, UT (United States)

Citations

IDCFRDescription
1807721 CFR 630.10(d)(2)Donation interval