FDA Inspection 669338 — Eisai Inc.

Eisai Inc. — FEI 1000158705

The FDA completed an inspection of Eisai Inc. on May 12, 2010 in Baltimore, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 12, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baltimore, MD (United States)