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FDA Inspection 1002541 — Alk-abello, Inc.

Alk-abello, Inc. — FEI 2431784

The FDA completed an inspection of Alk-abello, Inc. on December 21, 2016 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
December 21, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Port Washington, NY (United States)

Facility

Other inspections at this facility

  • 1220460 (VAI Tue Oct 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1202393 (VAI Thu Mar 09 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1070323 (VAI Tue Oct 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871138 (VAI Tue Feb 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 780215 (VAI Wed Mar 21 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources