FDA Inspection 1013806 — LG NewCorp

LG NewCorp — FEI 1270472

The FDA completed an inspection of LG NewCorp on May 5, 2017 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
May 5, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Methuen, MA (United States)