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FDA Inspection 780215 — Alk-abello, Inc.

Alk-abello, Inc. — FEI 2431784

The FDA completed an inspection of Alk-abello, Inc. on March 21, 2012 in Port Washington, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 21, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Port Washington, NY (United States)

Facility

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FDA data resources