FDA Inspection 988235 — GlaxoSmithKline LLC

GlaxoSmithKline LLC — FEI 1035048

The FDA completed an inspection of GlaxoSmithKline LLC on July 15, 2016 in Durham, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Durham, NC (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)