FDA Inspection 1062147 — Exelead, Inc.

Exelead, Inc. — FEI 1000517970

The FDA completed an inspection of Exelead, Inc. on Jul 30, 2018 in Indianapolis, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

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

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