FDA Inspection 892618 — ALK-Abello, Inc.

ALK-Abello, Inc. — FEI 3006900385

The FDA completed an inspection of ALK-Abello, Inc. on August 26, 2014 in Plainville, CT. 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
August 26, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Plainville, CT (United States)