FDA Inspection 825448 — HemoCue AB

HemoCue AB — FEI 3003044483

The FDA completed an inspection of HemoCue AB on Mar 20, 2013 in Angelholm. 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 20, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Angelholm (Sweden)