FDA Inspection 1086864 — ARUP Laboratories, Inc.

ARUP Laboratories, Inc. — FEI 3004741920

The FDA completed an inspection of ARUP Laboratories, Inc. on Mar 11, 2019 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 11, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Salt Lake City, UT (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.