FDA Inspection 1062147 — Exelead, Inc.

Exelead, Inc. — FEI 1000517970

The FDA completed an inspection of Exelead, Inc. on July 30, 2018 in Indianapolis, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 30, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Indianapolis, IN (United States)