FDA Inspection 935200 — LG NewCorp

LG NewCorp — FEI 1270472

The FDA completed an inspection of LG NewCorp on June 22, 2015 in Methuen, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 22, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Methuen, MA (United States)