FDA Inspection 952012 — Immucor, Inc.

Immucor, Inc. — FEI 1034569

The FDA completed an inspection of Immucor, Inc. on November 20, 2015 in Peachtree Corners, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 20, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Peachtree Corners, GA (United States)