FDA Inspection 1069321 — Quest Diagnostics

Quest Diagnostics — FEI 1872752

The FDA completed an inspection of Quest Diagnostics on Sep 13, 2018 in Indianapolis, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 13, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Indianapolis, IN (United States)